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Longer titles found: Hereditary spherocytosis (view)

searching for Spherocytosis 18 found (80 total)

SPTB (1,053 words) [view diff] exact match in snippet view article find links to article

PMID 2209094. "Entrez Gene: SPTB spectrin, beta, erythrocytic (includes spherocytosis, clinical type I)". Bennett V, Baines AJ (July 2001). "Spectrin and

Splenectomy (1,839 words) [view diff] exact match in snippet view article find links to article

deficiency Those who have a severe version of the hereditary blood disorder Spherocytosis. During surgical resection of a pancreatic cancer The classical cause

Cytosis (1,336 words) [view diff] no match in snippet view article find links to article

-Cytosis is a suffix that either refers to certain aspects of cells ie cellular process or phenomenon or sometimes refers to predominance of certain type

Splenic infarction (1,229 words) [view diff] exact match in snippet view article find links to article

infarction after Epstein-Barr virus infection in a patient with hereditary spherocytosis". Int. J. Hematol. 85 (5): 380–3. doi:10.1532/IJH97.07208. PMID 17562611

Hepatosplenomegaly (222 words) [view diff] exact match in snippet view article find links to article

Leukaemia Lymphoma Pernicious anaemia Sickle cell anaemia Hereditary Spherocytosis Thalassaemia Myelofibrosis Metabolic disease: Niemann-Pick disease Gaucher's

List of diseases (T) (849 words) [view diff] exact match in snippet view article

Tricho-hepato-enteric syndrome Trichomalacia Trichomegaly cataract hereditary spherocytosis Trichomegaly retina pigmentary degeneration dwarfi Trichomoniasis Trichoodontoonychial

Spectrin, alpha 1 (1,041 words) [view diff] exact match in snippet view article find links to article

Iolascon A, Miraglia del Giudice E, Perrotta S, et al. (1998). "Hereditary spherocytosis: from clinical to molecular defects". Haematologica. 83 (3): 240–57

Extramedullary hematopoiesis (1,806 words) [view diff] exact match in snippet view article find links to article

benign hematological disorders such as sickle cell anemia, hereditary spherocytosis, congenital dyserythroblastic anemia and idiopathic thrombocytopenic

Pleckstrin homology and rhogef domain containing g3 (141 words) [view diff] exact match in snippet view article find links to article

microdeletion on chromosome 14q23.2-23.3 in a patient with autism and spherocytosis". Autism Res. 4 (3): 221–7. doi:10.1002/aur.186. PMC 3110642. PMID 21360829

ADD3 (792 words) [view diff] exact match in snippet view article find links to article

"Targeted disruption of the β adducin gene (Add2) causes red blood cell spherocytosis in mice". Proc. Natl. Acad. Sci. U.S.A. 96 (19): 10717–22. Bibcode:1999PNAS

Protein 4.2 (978 words) [view diff] exact match in snippet view article find links to article

the erythrocyte protein 4.2 gene of Japanese patients with hereditary spherocytosis (protein 4.2 Fukuoka)". Br. J. Haematol. 88 (3): 527–533. doi:10.1111/j

List of MeSH codes (C15) (3,000 words) [view diff] exact match in snippet view article

071.141.150.490 – hemoglobin c disease MeSH C15.378.071.141.150.785 – spherocytosis, hereditary MeSH C15.378.071.141.150.875 – thalassemia MeSH C15.378

Gilbert's syndrome (3,717 words) [view diff] exact match in snippet view article find links to article

increases the risk for developing gallstones in patients with hereditary spherocytosis". Blood. 94 (7): 2259–62. doi:10.1182/blood.V94.7.2259.419k42_2259_2262

Ankyrin-2 (3,706 words) [view diff] exact match in snippet view article find links to article

"Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis". Nature Genetics. 13 (2): 214–8. doi:10.1038/ng0696-214. PMID 8640229

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

PHL Pranke, "Red cell membrane protein abnormalities in hereditary spherocytosis in Brazil." British journal of haematology 88 (2), (1994): 295-299 Pranke

List of diseases (C) (3,648 words) [view diff] exact match in snippet view article

familial Cardiomyopathy hypogonadism metabolic anomalies Cardiomyopathy spherocytosis Cardiomyopathy, fatal fetal, due to myocardial calcification Cardiomyopathy

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

FOXP2 Spherocytosis, hereditary, type 5; 612690; EPB42 Spherocytosis, type 1; 182900; ANK1 Spherocytosis, type 3; 270970; SPTA1 Spherocytosis, type 4;

List of MeSH codes (C16) (6,496 words) [view diff] exact match in snippet view article

MeSH C16.320.070.490 – hemoglobin c disease MeSH C16.320.070.785 – spherocytosis, hereditary MeSH C16.320.070.875 – thalassemia MeSH C16.320.070.875