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Longer titles found: Mucopolysaccharidosis type I (view)

searching for mucopolysaccharidosis 33 found (85 total)

alternate case: Mucopolysaccharidosis

Galactosamine-6 sulfatase (967 words) [view diff] exact match in snippet view article find links to article

sulfatase (Morquio syndrome, mucopolysaccharidosis type IVA)". Fukuda S, Tomatsu S, Masue M, et al. (1992). "Mucopolysaccharidosis type IVA. N-acetylgalactosamine-6-sulfate
Arylsulfatase B (1,427 words) [view diff] exact match in snippet view article find links to article
4-sulfate sulfohydrolase, EC 3.1.6.12) is an enzyme associated with mucopolysaccharidosis VI (Maroteaux–Lamy syndrome). Arylsulfatase B is among a group of
Acromicric dysplasia (101 words) [view diff] exact match in snippet view article find links to article
with Geleophysic dysplasia (or Geleophysic Dwarfism) and Focal mucopolysaccharidosis. "Acromicric dysplasia | Genetic and Rare Diseases Information Center
Luis Morquio (296 words) [view diff] exact match in snippet view article find links to article
physician and professor. A medical condition, Morquio syndrome (mucopolysaccharidosis IV), is named in his honor. Morquio was born on September 24, 1867
SGSH (1,132 words) [view diff] exact match in snippet view article find links to article
sulfohydrolase (SGSH; MIM 605270). The Sanfilippo syndrome, or mucopolysaccharidosis III, is a lysosomal storage disease due to impaired degradation
Vestronidase alfa-vjbk (581 words) [view diff] exact match in snippet view article find links to article
and adult patients with an inherited metabolic condition called mucopolysaccharidosis type VII (MPS VII), also known as Sly syndrome. MPS VII is an extremely
Iduronidase (1,864 words) [view diff] exact match in snippet view article find links to article
Aldurazyme was granted orphan designation for Treatment of patients with mucopolysaccharidosis-I on September 24, 1997. As of 2014, Aldurazyme was mandated to
VPS33A (553 words) [view diff] exact match in snippet view article find links to article
with mutations in this gene. This syndrome has since been named Mucopolysaccharidosis-plus syndrome. GRCm38: Ensembl release 89: ENSMUSG00000029434 -
List of MeSH codes (C18) (4,274 words) [view diff] exact match in snippet view article
715.640 – mucopolysaccharidosis I MeSH C18.452.648.202.715.645 – mucopolysaccharidosis II MeSH C18.452.648.202.715.650 – mucopolysaccharidosis III MeSH
HYAL1 (2,031 words) [view diff] exact match in snippet view article find links to article
hyaluronidase in plasma. Mutations in this gene are associated with mucopolysaccharidosis type IX, or hyaluronidase deficiency. The gene is one of several
List of MeSH codes (C16) (6,496 words) [view diff] exact match in snippet view article
715.640 – mucopolysaccharidosis I MeSH C16.320.565.202.715.645 – mucopolysaccharidosis II MeSH C16.320.565.202.715.650 – mucopolysaccharidosis III MeSH
Hydrops fetalis (698 words) [view diff] exact match in snippet view article find links to article
deficiency is the cause of the lysosomal storage disease called mucopolysaccharidosis type VII. Congenital disorders of glycosylation Parvovirus B19 (fifth
Short stature (1,553 words) [view diff] exact match in snippet view article find links to article
which there is trunk shortening as spondyloepiphyseal dysplasia and mucopolysaccharidosis Short-limb short stature can be further subcategorised in accordance
Schipperke (1,146 words) [view diff] exact match in snippet view article find links to article
p. 2 University of Pennsylvania, School of Veterinary Medicine, Mucopolysaccharidosis IIB (MPS IIIB), 2008 University of Pennsylvania, School of Veterinary
GM1 gangliosidoses (554 words) [view diff] exact match in snippet view article find links to article
involvement but severe dysostosis resembling Morquio disease type A (Mucopolysaccharidosis type 4). Onset of late infantile GM1 is typically between ages 1
Epiphysiodesis (1,056 words) [view diff] exact match in snippet view article find links to article
(June 2015). "Characterization of knee alignment in children with mucopolysaccharidosis types I and II and outcome of treatment with guided growth". Journal
List of skin conditions (17,683 words) [view diff] exact match in snippet view article find links to article
(gargoylism, mucopolysaccharidosis type I) Hurler–Scheie syndrome (mucopolysaccharidosis type I H-S) Hyaluronidase deficiency (mucopolysaccharidosis type IX)
Osteochondrodysplasia (1,343 words) [view diff] exact match in snippet view article find links to article
(MPS) constitute a commonly seen group of osteochondrodysplasias. Mucopolysaccharidosis can cause a wide spectrum of clinical and radiologic manifestations
HYAL3 (448 words) [view diff] exact match in snippet view article find links to article
hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IX". Proc. Natl. Acad. Sci. U.S.A. 96 (11): 6296–300. doi:10.1073/pnas
List of MeSH codes (C17) (3,128 words) [view diff] exact match in snippet view article
550.575.640 – mucopolysaccharidosis i MeSH C17.300.550.575.645 – mucopolysaccharidosis ii MeSH C17.300.550.575.650 – mucopolysaccharidosis iii MeSH C17
Chromosome 7 (2,616 words) [view diff] exact match in snippet view article find links to article
needed] maturity onset diabetes of the young type 3[citation needed] mucopolysaccharidosis type VII or Sly syndrome Muscular dystrophy, limb-girdle, type 1D
Portal hypertension (1,735 words) [view diff] exact match in snippet view article find links to article
of Disse Granulomatous or infiltrative liver diseases (Gaucher, mucopolysaccharidosis, sarcoidosis, lymphoproliferative malignancies, amyloid deposition
Alpha-mannosidosis (1,570 words) [view diff] exact match in snippet view article find links to article
shared with those of other lysosomal storage disorders, such as mucopolysaccharidosis. Given the progressive nature of the disease, the earlier a correct
Elosulfase alfa (417 words) [view diff] exact match in snippet view article find links to article
therapy with BMN 110 (elosulfase alfa) for Morquio A syndrome (mucopolysaccharidosis IVA): a phase 3 randomised placebo-controlled study". Journal of
List of OMIM disorder codes (18,858 words) [view diff] exact match in snippet view article find links to article
MCOLN1 Mucopolysaccharidosis Ih; 607014; IDUA Mucopolysaccharidosis Ih/s; 607015; IDUA Mucopolysaccharidosis Is; 607016; IDUA Mucopolysaccharidosis IVA;
Leonard M. Miller School of Medicine (2,527 words) [view diff] exact match in snippet view article find links to article
neuroscience as well as programs centered on a variety of targets in mucopolysaccharidosis, addiction, schizophrenia, fragile X, obesity, Alzheimer's, Parkinson's
Helge Stormorken (2,022 words) [view diff] exact match in snippet view article find links to article
Erik; Stormorken, Helge (28 June 2008). "Concomitant occurrence of mucopolysaccharidosis IIIB and Glanzmann's thrombasthenia. Further evidence of a hyperactive 
Priority review (3,258 words) [view diff] exact match in snippet view article find links to article
ChemoResearch Rare pediatric Kymriah B-ALL Novartis Rare pediatric Mepsevii Mucopolysaccharidosis type VII Ultragenyx Rare pediatric Luxturna RPE65-mutated retinal
Daniel Berger (physician) (1,650 words) [view diff] exact match in snippet view article
cardiovascular and pulmonary outcomes of World Trade Center exposure, mucopolysaccharidosis, Pompe's Disease and pulmonary manifestations of obesity (http://www
List of geneticists (7,533 words) [view diff] exact match in snippet view article find links to article
heredity William S. Sly (born c. 1931), US biochemical geneticist, mucopolysaccharidosis type VII (Sly syndrome) Cedric A. B. Smith (1917–2002), British
William S. Sly (868 words) [view diff] exact match in snippet view article find links to article
report of clinical, radiologic, and biochemical features of a new mucopolysaccharidosis". J. Pediatr. 82 (2): 249–57. doi:10.1016/S0022-3476(73)80162-3
Flat-chested kitten syndrome (5,304 words) [view diff] exact match in snippet view article find links to article
Gardner, S. A., Owens, J. M., Wenger, D. A., Thrall, M. A. (2000). Mucopolysaccharidosis VII in a cat. Veterinary Pathology 37, 502–505. Shires, PK, Waldron
List of MeSH codes (C10) (9,229 words) [view diff] exact match in snippet view article
687 – menkes kinky hair syndrome MeSH C10.597.606.643.455.750 – mucopolysaccharidosis ii MeSH C10.597.606.643.455.875 – pyruvate dehydrogenase complex