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Longer titles found: Neurofibromatosis type 3 (view), Neurofibromatosis type 4 (view), Neurofibromatosis type I (view), Neurofibromatosis type II (view)

searching for Neurofibromatosis 104 found (328 total)

alternate case: neurofibromatosis

Lisch nodule (340 words) [view diff] exact match in snippet view article find links to article

(Riccardi VM: Von Recklinghausen Neurofibromatosis. N Engl J Med 1981;305:1617-27). These nodules are found in neurofibromatosis type 1, and are present in

SPTBN1 (997 words) [view diff] exact match in snippet view article find links to article

Crompton MR (September 2001). "Binding of the merlin-I product of the neurofibromatosis type 2 tumour suppressor gene to a novel site in beta-fodrin is regulated

List of radiographic findings associated with cutaneous conditions (165 words) [view diff] exact match in snippet view article find links to article

Myxoid cyst Exostosis Proteus syndrome Scoliosis Ichthyosis hystrix Neurofibromatosis type 1 Proteus syndrome Distal phalangeal radiolucency Incontinentia

EVI2B (472 words) [view diff] exact match in snippet view article find links to article

genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 gene". Genomics. 9 (3): 446–60. doi:10.1016/0888-7543(91)90410-G

Intraneural perineurioma (362 words) [view diff] exact match in snippet view article find links to article

chromosome 22, intraneural perineurioma has not been associated with neurofibromatosis. Due to the involvement of one or more nerve fascicles, intraneural

Genetic disorder (3,560 words) [view diff] exact match in snippet view article find links to article

this type of disorder are Huntington's disease,: 58 neurofibromatosis type 1, neurofibromatosis type 2, Marfan syndrome, hereditary nonpolyposis colorectal

List of genes mutated in cutaneous conditions (108 words) [view diff] exact match in snippet view article find links to article

MCR1R Red hair color Menin (MENI) MEN1A (Wermer syndrome) Merlin Neurofibromatosis type 2 Merosin Infantile hemangioma MLH1 Muir–Torre syndrome MLPH

RNF135 (551 words) [view diff] exact match in snippet view article find links to article

chromosomal region known to be frequently deleted in patients with neurofibromatosis. Alternatively spliced transcript variants encoding distinct isoforms

Pacak–Zhuang syndrome (696 words) [view diff] exact match in snippet view article find links to article

carrying hereditary syndromes like multiple endocrine neoplasia (MEN), neurofibromatosis 1 (NF1), or von Hippel-Lindau (VHL) disease. Mutations in the genes

Juvenile myelomonocytic leukemia (2,981 words) [view diff] exact match in snippet view article find links to article

show common nonspecific signs and symptoms. Children with JMML and neurofibromatosis 1 (NF1) (about 14% of children with JMML are also clinically diagnosed

Rosalie Ferner (199 words) [view diff] exact match in snippet view article find links to article

with neurofibromatosis 1." Journal of medical genetics 44, no. 2 (2007): 81-88. doi:10.1136/jmg.2006.045906 Ferner, Rosalie E. "Neurofibromatosis 1 and

Acute lymphoblastic leukemia (7,663 words) [view diff] exact match in snippet view article find links to article

risk factors may include Down syndrome, Li–Fraumeni syndrome, or neurofibromatosis type 1. Environmental risk factors may include significant radiation

Shlomi Constantini (184 words) [view diff] exact match in snippet view article find links to article

University, he is also the director of the Gilbert International Neurofibromatosis Center. Constantini first trained in Hadassah Medial Center, Jerusalem

List of MeSH codes (G14) (3,088 words) [view diff] exact match in snippet view article

MeSH G14.340.024.340.383.249.340 – genes, neurofibromatosis 1 MeSH G14.340.024.340.383.249.345 – genes, neurofibromatosis 2 MeSH G14.340.024.340.383.249.375

List of conditions associated with café au lait macules (185 words) [view diff] exact match in snippet view article find links to article

McCune–Albright syndrome Multiple endocrine neoplasia type 1 Neurofibromatosis type 1 Neurofibromatosis type 1-like syndrome Noonan syndrome Peutz–Jeghers syndrome

Nodule (medicine) (702 words) [view diff] exact match in snippet view article

on vocal cords, They occur in conditions including endometriosis, neurofibromatosis, and in rheumatoid arthritis. They may also feature in Kaposi's sarcoma

Penetrance (2,413 words) [view diff] exact match in snippet view article find links to article

associated trait, the genotype is said to show complete penetrance. Neurofibromatosis type 1 (NF1), is an autosomal dominant condition which shows complete

List of MeSH codes (C09) (576 words) [view diff] exact match in snippet view article

218.807.800.675 – neuroma, acoustic MeSH C09.218.807.800.675.500 – neurofibromatosis 2 MeSH C09.218.807.800.837 – vestibular neuronitis MeSH C09.400.535

D. Wade Clapp (522 words) [view diff] exact match in snippet view article find links to article

Gleevec had the possibility to be the first effective therapy for neurofibromatosis type 1 tumor. Following this, Clapp was named the Chairman of the

SR protein (3,445 words) [view diff] exact match in snippet view article find links to article

proteins can increase translation of mRNA. Ataxia telangiectasia, neurofibromatosis type 1, several cancers, HIV-1, and spinal muscular atrophy have all

List of medical mnemonics (3,990 words) [view diff] no match in snippet view article find links to article

This is a list of mnemonics used in medicine and medical science, categorized and alphabetized. A mnemonic is any technique that assists the human memory

Gareth Evans (geneticist) (351 words) [view diff] exact match in snippet view article

an MD in cancer genetics developing his career specialisation in neurofibromatosis type 2, while working as a Senior Clinical Research Fellow at Manchester

PAK2 (2,164 words) [view diff] exact match in snippet view article find links to article

inhibits PAK2 and PAK1 activities; FRAX597 suppresses PAK2 activity in neurofibromatosis type 2 (NF2)-associated tumorigenesis; and miR-23b and miR-137 inhibits

List of abbreviations for diseases and disorders (112 words) [view diff] exact match in snippet view article find links to article

coronavirus-infected pneumonia NCL Neuronal ceroid lipofuscinosis NF1 Neurofibromatosis type 1 NF2 Neurofibromatosis type 2 NKH Nonketotic hyperglycinemia NLD Nonverbal

Spinal disease (3,055 words) [view diff] exact match in snippet view article find links to article

that may affect spinal tumors, include Von Hippel-Lindau disease and Neurofibromatosis 2. Von Hippel-Lindau disease is a non-cancerous tumor of blood vessels

James F. Gusella (845 words) [view diff] exact match in snippet view article find links to article

lab employed similar strategies to identify genes responsible for neurofibromatosis type 2 and a familial form of Alzheimer's disease. In 1999, along

Amita Sehgal (2,065 words) [view diff] exact match in snippet view article find links to article

Neurofibromin 1 (NF1) is a tumor suppressor gene known to be dis-regulated in Neurofibromatosis type 1, a disorder which causes tumors along the spine. In 2001, Sehgal

HGS (gene) (1,399 words) [view diff] exact match in snippet view article

Huynh DP, Chen MS, Burke SP, Gutmann DH, Pulst SM (July 2000). "The neurofibromatosis 2 tumor suppressor protein interacts with hepatocyte growth factor-regulated

Moyamoya disease (3,406 words) [view diff] exact match in snippet view article find links to article

congenital or acquired. Patients with Down syndrome, sickle cell anemia, neurofibromatosis type 1, congenital heart disease, fibromuscular dysplasia, activated

KIF5B (1,036 words) [view diff] exact match in snippet view article find links to article

kinesin-1 links neurofibromin and merlin in a common cellular pathway of neurofibromatosis". The Journal of Biological Chemistry. 277 (40): 36909–12. doi:10

Synovial sarcoma (1,443 words) [view diff] exact match in snippet view article find links to article

t(X;18)-Negative Sarcomas. Molecular Analysis of 25 Cases Occurring in Neurofibromatosis Type 1 Patients, Using Two Different RT-PCR-Based Methods of Detection"

Moyamoya disease (3,406 words) [view diff] exact match in snippet view article find links to article

congenital or acquired. Patients with Down syndrome, sickle cell anemia, neurofibromatosis type 1, congenital heart disease, fibromuscular dysplasia, activated

Caffeic acid phenethyl ester (428 words) [view diff] exact match in snippet view article find links to article

ester)-based propolis extract (Bio 30) suppresses the growth of human neurofibromatosis (NF) tumor xenografts in mice". Phytother Res. 23 (2): 226–30. doi:10

Oral mucosa (4,303 words) [view diff] exact match in snippet view article find links to article

multiple lesions associated with (Von Reckllinghausen's Disease) neurofibromatosis (4). They can be preceded by café au lait pigmentation spots on the

Glossary of communication disorders (3,554 words) [view diff] exact match in snippet view article find links to article

and/or dizziness. (sometimes called vestibular schwannoma). Also see Neurofibromatosis Type 2. Acquired deafness Loss of hearing that occurs or develops

ICAM2 (1,211 words) [view diff] exact match in snippet view article find links to article

Rouleau GA, Jääskeläinen J, Vaheri A, Carpén O (September 1997). "Neurofibromatosis 2 tumor suppressor protein colocalizes with ezrin and CD44 and associates

TBPL1 (1,000 words) [view diff] exact match in snippet view article find links to article

functional regulator of transcription: reciprocal regulation of the neurofibromatosis type 1 and c-fos genes by TLF/TRF2 and TBP". Molecular and Cellular

Mismatch repair cancer syndrome (622 words) [view diff] exact match in snippet view article find links to article

malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1". European Journal of Human Genetics. 16 (1): 62–72. doi:10

Bruce R. Korf (771 words) [view diff] exact match in snippet view article find links to article

the new Chairman of the Medical Affairs Committee for the National Neurofibromatosis Foundation. Following this, Korf was named president-elect of the

Carolyn Farb (643 words) [view diff] exact match in snippet view article find links to article

Frida Kahlo Carolyn Farb Papers, 1955-2002 "Leading Scientist in Neurofibromatosis-Related Cancer to be Featured in Carolyn Farb Endowed Lecture - M

PAK3 (1,015 words) [view diff] exact match in snippet view article find links to article

inhibitor of the p21-activated kinases, inhibits tumorigenesis of neurofibromatosis type 2 (NF2)-associated Schwannomas". The Journal of Biological Chemistry

CRYBB2 (983 words) [view diff] exact match in snippet view article find links to article

beta B2 and beta B3 crystallin genes to 22q11.2----q12: markers for neurofibromatosis 2". Cytogenet. Cell Genet. 56 (3–4): 171–5. doi:10.1159/000133080

Gangliocytic paraganglioma (206 words) [view diff] exact match in snippet view article find links to article

tumour and paraganglioma. GPs may be sporadic or arise in the context neurofibromatosis type 1. Intermed. mag. Intermed. mag. Very high mag. Very high mag

Papillomatosis of breasts (2,023 words) [view diff] exact match in snippet view article find links to article

with BP are Cowden disease, Noonan syndrome, Proteus syndrome, and neurofibromatosis type 1. At their surgical excision, PB lesions grossly appear as tumors

APOBEC (751 words) [view diff] exact match in snippet view article find links to article

in the site-specific deamination of a CGA to a UGA stop codon in neurofibromatosis type 1 (NF1) mRNA, the resulting proteins are predicted to be truncated

Chromosome 22 (2,206 words) [view diff] exact match in snippet view article find links to article

Li-Fraumeni syndrome Metachromatic leukodystrophy Methemoglobinemia Neurofibromatosis type 2 Opitz G/BBB syndrome Renal medullary carcinoma Rubinstein-Taybi

Malignant triton tumor (206 words) [view diff] exact match in snippet view article find links to article

a peripheral nerve, or in a ganglioneuroma, or in a patient with neurofibromatosis type 1 (NF1), or has a metastatic character. The growth characteristics

Karl Lisch (162 words) [view diff] exact match in snippet view article find links to article

President of Austria in 1989, the Medal of Honor from the American Neurofibromatosis Society in 1992, and the First Class Cross Honor for Science and the

Shashanka Koirala (683 words) [view diff] exact match in snippet view article find links to article

S. Koirala, J. Inst. Med., P. 277–282, 1986. 2. Von 's disease (Neurofibromatosis): Case report: P.C. Karmacharya, S. Koirala, M.P. Upadhyay J. Inst

Terry Fator (2,456 words) [view diff] exact match in snippet view article find links to article

2010, Fator did a doodle for a charity celebrity doodle auction for Neurofibromatosis, more commonly known as NF. 100% of the profit from all the doodles

Corynebacterium macginleyi (252 words) [view diff] exact match in snippet view article find links to article

"Surgical Site Infection by Corynebacterium macginleyi in a Patient with Neurofibromatosis Type 1". Case Reports in Infectious Diseases. 2013: 1–3. doi:10.1155/2013/970678

Wladimir Wertelecki (3,592 words) [view diff] exact match in snippet view article find links to article

: Diagnosis of NF-2. In: Neurofibromatosis 2. Eds., Cohen, B.R. Korf, B.H., Pugh, J.N., The National Neurofibromatosis Foundation, Inc., New York,

FERM domain (774 words) [view diff] exact match in snippet view article find links to article

N-terminal domain crystal structure of the ferm domain of merlin, the neurofibromatosis 2 tumor suppressor protein. Identifiers Symbol FERM_N Pfam PF09379

OMG (gene) (604 words) [view diff] exact match in snippet view article

encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 gene". Mol Cell Biol. 11 (2): 906–12. doi:10.1128/mcb.11.2

Dentate nucleus (2,529 words) [view diff] exact match in snippet view article find links to article

dentate nucleus is not affected until late in disease progression. Neurofibromatosis type 1 (NF1): NF1 is an autosomal dominant neurocutaneous disorder

Siphunculina (424 words) [view diff] exact match in snippet view article find links to article

(2):111–121 Brownstein S, Bernardo AI, Suprapto, Salim I. (1976) Neurofibromatosis with the eye fly Siphunculina funicola in an eyelid tumor. Can J Ophthalmol

CASK (2,890 words) [view diff] exact match in snippet view article find links to article

Sheng M, Roberts RG (June 2001). "Bipartite interaction between neurofibromatosis type I protein (neurofibromin) and syndecan transmembrane heparan

APOBEC1 (2,785 words) [view diff] exact match in snippet view article find links to article

RM, Kennedy S, Viskochil D, Davidson NO (2002). "C-->U editing of neurofibromatosis 1 mRNA occurs in tumors that express both the type II transcript and

SUZ12 (1,230 words) [view diff] exact match in snippet view article find links to article

(September 2004). "High frequency of mosaicism among patients with neurofibromatosis type 1 (NF1) with microdeletions caused by somatic recombination of

NFLS (61 words) [view diff] exact match in snippet view article find links to article

located in Nanjing, Jiangsu, China Legius syndrome, also known as Neurofibromatosis 1-like syndrome, a genetic disorder This disambiguation page lists

Jim Rice (3,857 words) [view diff] exact match in snippet view article find links to article

dedication to cancer research. Rice is also active in his support of the Neurofibromatosis Foundation of New England. Rice's involvement with Major League Baseball's

SGCG (1,820 words) [view diff] exact match in snippet view article find links to article

Viskochil D, O'Connell P, Ward K (1993). "Linkage disequilibrium in the neurofibromatosis 1 (NF1) region: implications for gene mapping". Am. J. Hum. Genet

Crystallin, beta A1 (1,047 words) [view diff] exact match in snippet view article find links to article

beta B2 and beta B3 crystallin genes to 22q11.2----q12: markers for neurofibromatosis 2". Cytogenet. Cell Genet. 56 (3–4): 171–5. doi:10.1159/000133080

Jacob Wesley Ulm (1,454 words) [view diff] exact match in snippet view article find links to article

annual Neurofibromatosis Prize for Research Ideas competition, sponsored by National Neurofibromatosis Foundation and the International Neurofibromatosis Association

Cerebellopontine angle syndrome (1,155 words) [view diff] exact match in snippet view article find links to article

developing an acoustic neuroma is having a rare genetic condition called neurofibromatosis type 2 (NF2). There are no confirmed environmental risk factors for

GTPBP4 (578 words) [view diff] exact match in snippet view article find links to article

tumor suppressor NGB, a GTP-binding protein that interacts with the neurofibromatosis 2 protein". Mol. Cell. Biol. 27 (6): 2103–19. doi:10.1128/MCB.00572-06

Ezrin (1,381 words) [view diff] exact match in snippet view article find links to article

Carpén O (March 1999). "Homotypic and heterotypic interaction of the neurofibromatosis 2 tumor suppressor protein merlin and the ERM protein ezrin". J. Cell

RAB11FIP4 (617 words) [view diff] exact match in snippet view article find links to article

characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions". Am J Hum Genet. 69 (3): 516–527

Peter Tishler (954 words) [view diff] exact match in snippet view article find links to article

P. V. (Sep 1975). "A family with coexistent von Recklinghausen's neurofibromatosis and von Hippel-Lindau's disease. Diseases possibly derived from a

Bruce Ponder (2,395 words) [view diff] exact match in snippet view article find links to article

(1990), the International Public Service Award of the US National Neurofibromatosis Association (1992), the Merck Prize of the European Thyroid Association

Luis Parada (neuroscientist) (695 words) [view diff] exact match in snippet view article

laboratory uses genetic mouse models to study human disease including Neurofibromatosis, cancers of the nervous system, cancer stem cells, autism, and neural

Pancreatic neuroendocrine tumor (2,443 words) [view diff] exact match in snippet view article find links to article

of multiple endocrine neoplasia type 1, Von Hippel–Lindau disease, neurofibromatosis type 1 (NF-1) or tuberose sclerosis (TSC) Analysis of somatic DNA

Bruce Ponder (2,395 words) [view diff] exact match in snippet view article find links to article

(1990), the International Public Service Award of the US National Neurofibromatosis Association (1992), the Merck Prize of the European Thyroid Association

Luis Parada (neuroscientist) (695 words) [view diff] exact match in snippet view article

laboratory uses genetic mouse models to study human disease including Neurofibromatosis, cancers of the nervous system, cancer stem cells, autism, and neural

Hippo signaling pathway (3,130 words) [view diff] exact match in snippet view article find links to article

PMC 2667156. PMID 19048595. Evans DG, Sainio M, Baser ME (December 2000). "Neurofibromatosis type 2". Journal of Medical Genetics. 37 (12): 897–904. doi:10.1136/jmg

ThriftyComputer (334 words) [view diff] exact match in snippet view article find links to article

significant challenges. Since infancy, Elchonon Hellinger has suffered from Neurofibromatosis Type 2, which causes the continuous growth of benign tumors. By the

Cataract (6,616 words) [view diff] exact match in snippet view article find links to article

18 (Edward's syndrome), and Turner's syndrome, and in the case of neurofibromatosis type 2, juvenile cataract on one or both sides may be noted. Examples

NLK (1,049 words) [view diff] exact match in snippet view article find links to article

"Characterization of the Fugu rubripes NLK and FN5 genes flanking the NF1 (Neurofibromatosis type 1) gene in the 5' direction and mapping of the human counterparts"

List of diseases (S) (1,934 words) [view diff] exact match in snippet view article

Seemanova–Lesny syndrome Seemanova syndrome type 2 Seghers syndrome Segmental neurofibromatosis Segmental vertebral anomalies Seizures benign familial neonatal recessive

Periannan Senapathy (4,081 words) [view diff] exact match in snippet view article find links to article

mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1". Human Molecular Genetics. 9 (2): 237–247. doi:10.1093/hmg/9

DLK1 (1,303 words) [view diff] exact match in snippet view article find links to article

factor superfamily, in neurofibromas and serum from patients with neurofibromatosis type 1". British Journal of Dermatology. 140 (6): 1054–9. doi:10.1046/j

Neuregulin 1 (3,921 words) [view diff] exact match in snippet view article find links to article

maturation, survival, and motility, important in research related to neurofibromatosis type two (NF2).[citation needed] Neuregulin-1 (NRG-1), a cardioactive

Deepak Agrawal (1,614 words) [view diff] exact match in snippet view article find links to article

Preservation After Gamma Knife Radiosurgery for Vestibular Schwannomas in Neurofibromatosis Type 2-A Retrospective Analysis of 133 Tumors". National Medical Library

Inspire (company) (1,592 words) [view diff] exact match in snippet view article

Liver Foundation, Lupus Foundation of America, Encephalitis Global, Neurofibromatosis Network, American Sexual Health Association, Ehlers-Danlos Society

Bevacizumab (7,144 words) [view diff] exact match in snippet view article find links to article

(August 2012). "Bevacizumab for progressive vestibular schwannoma in neurofibromatosis type 2: a retrospective review of 31 patients" (PDF). Otology & Neurotology

SMCO4 (639 words) [view diff] exact match in snippet view article find links to article

"Characterization of the Fugu rubripes NLK and FN5 genes flanking the NF1 (Neurofibromatosis type 1) gene in the 5' direction and mapping of the human counterparts"

Hearing loss (10,963 words) [view diff] exact match in snippet view article find links to article

Stickler syndrome, Waardenburg syndrome, Alport's syndrome, and neurofibromatosis type 2. Nonsyndromic deafness occurs when there are no other signs

Gelareh Zadeh (755 words) [view diff] exact match in snippet view article find links to article

works with Vera Bril on the University Health Network Elizabeth Raab Neurofibromatosis Program. Zadeh was the first woman to be elected Chair of the Division

THOC5 (1,483 words) [view diff] exact match in snippet view article find links to article

anonymous gene from a megabase-range YAC and cosmid contig in the neurofibromatosis type 2/meningioma region on human chromosome 22q12". Hum Mol Genet

Alison Lloyd (357 words) [view diff] exact match in snippet view article find links to article

peripheral nervous system" and "an influential member of the international Neurofibromatosis community". She was elected Fellow of the Academy of Medical Sciences

BioGeM (1,003 words) [view diff] exact match in snippet view article find links to article

et al. (2019). "The molecular landscape of glioma in patients with Neurofibromatosis 1". Nature Medicine. 25 (1): 176–187. doi:10.1038/s41591-018-0263-8

Scream Queens season 2 (1,506 words) [view diff] exact match in snippet view article find links to article

slaughtered every single person inside. A man named Tyler, suffering from Neurofibromatosis (a collection of tumours all over his body), comes to the hospital

List of diseases (C) (3,643 words) [view diff] exact match in snippet view article

protozoal infections Central serous chorioretinopathy Central type neurofibromatosis Centromeric instability immunodeficiency syndrome Centronuclear myopathy

William Schull (2,060 words) [view diff] exact match in snippet view article find links to article

V. (1956) A Clinical, Pathological and Genetic Study of Multiple Neurofibromatosis. Springfield, Ill.: C. C. Thomas. Neel, J. V. and Schull, W. J. (1956)

Pheochromocytoma (16,172 words) [view diff] exact match in snippet view article find links to article

MEN2 (Multiple Endocrine Neoplasia-2); VHL (von-Hippel Lindau); NF1 (Neurofibromatosis-1); NET (Neuroendocrine Tumor); CNS (Central Nervous System) SDHx

Mechanography (2,920 words) [view diff] exact match in snippet view article find links to article

Mughal MZ.: Vitamin D status and muscle function in children with neurofibromatosis type 1 (NF1)., J Musculoskelet Neuronal Interact., 13(1):111-119,

Lillian Glass (3,121 words) [view diff] exact match in snippet view article find links to article

Lillian; Riccardi, Vincent M. (1981). "Speech and Von Recklinghausen Neurofibromatosis". New England Journal of Medicine. 305 (27): 1617–1626. doi:10

2018 Birthday Honours (14,943 words) [view diff] exact match in snippet view article find links to article

Cook, Founding Director, Can You Hear Us? For voluntary services to Neurofibromatosis Type 2 Patients. Lowri Ann, Mrs. Cope. For services to the community

List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article

EWSR1 Neurofibromatosis, familial spinal; 162210; NF1 Neurofibromatosis type 1; 162200; NF1 Neurofibromatosis type 2; 101000; NF2 Neurofibromatosis-Noonan

2006 Birthday Honours (17,765 words) [view diff] exact match in snippet view article find links to article

HM Revenue and Customs. Clare Margaret Webb, Co-Founder and Chair, Neurofibromatosis Association. For services to Healthcare. Lulie Webb. For charitable

List of True Life episodes (3,217 words) [view diff] exact match in snippet view article find links to article

(3/29/2010) (208) "I'm Relocating for Love" (4/5/2010) (209) "I Have Neurofibromatosis" (4/12/2010) (210) "I Hate My Face" (4/19/2010) (211) "I'm Hustling

Causes of hearing loss (4,407 words) [view diff] exact match in snippet view article find links to article

Waardenburg syndrome, Chudley-Mccullough syndrome, Alport's syndrome, and neurofibromatosis type 2. These are diseases that have deafness as one of the symptoms

Paul Billings (3,777 words) [view diff] exact match in snippet view article find links to article

Understanding the EEC split. GeneLetter 2000; 1 (Feb); 1) Thinking in neurofibromatosis type 1. (GeneLetter 2000, 1) Constructing new genetics. GeneLetter

List of women neuroscientists (8,913 words) [view diff] exact match in snippet view article find links to article

neurologist, and clinical geneticist working on cognitive deficits in neurofibromatosis type 1 and intervention strategies for children with learning disabilities