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Results 101 - 110 of 120 for Blood group B
  1. PMM2-congenital disorder of glycosylation 
    ... de Lonlay P, Seta N, Barrot S, Chabrol B, Drouin V, Gabriel BM, Journel H, Kretz M, ... Monin ML, Mignot C, De Lonlay P, Heron B, Masurel A, Mathieu-Dramard M, Lenaerts C, Thauvin ...
    https://medlineplus.gov/...pmm2-congenital-disorder-of-glycosylation - Genetics
  2. Russell-Silver syndrome 
    ... AP, Chrzanowska KH, Davies JH, Dias RP, Dubern B, Elbracht M, Giabicani E, Grimberg A, Gronskov K, ...
    https://medlineplus.gov/genetics/condition/russell-silver-syndrome - Genetics
  3. Adenine phosphoribosyltransferase deficiency 
    ... urinary tract stones include fever, urinary tract infection, blood in the urine (hematuria), abdominal cramps, nausea, and ... M, Ceballos-Picot I, Bensman A; APRT Study Group. Adenine phosphoribosyltransferase deficiency in children. Pediatr Nephrol. 2012 ...
    https://medlineplus.gov/...nine-phosphoribosyltransferase-deficiency - Genetics
  4. Renal tubular acidosis with deafness 
    ... H+-ATPase (V-ATPase). V-ATPases are a group of similar complexes that act as pumps to ... also known as a glomerulus) that filters the blood, and a renal tubule that reabsorbs substances that ...
    https://medlineplus.gov/.../renal-tubular-acidosis-with-deafness - Genetics
  5. Early-onset isolated dystonia 
    ... No abstract available. Citation on PubMed Breakefield XO, Blood AJ, Li Y, Hallett M, Hanson PI, Standaert ...
    https://medlineplus.gov/.../condition/early-onset-isolated-dystonia - Genetics
  6. Saul-Wilson syndrome 
    ... intelligence.In Saul-Wilson syndrome, levels of white blood cells can vary from normal to low (intermittent ... Taylan F, Sharma P, Turgeon CT, Blanco-Sanchez B, Ng BG, Logan CV, Wolfe LA, Solomon BD, ...
    https://medlineplus.gov/genetics/condition/saul-wilson-syndrome - Genetics
  7. Amish lethal microcephaly 
    ... to develop elevated levels of acid in the blood and tissues (metabolic acidosis). Infants with this disorder ... 1002/ajmg.a.33373. Citation on PubMed Tabarki B, Thabet F, Alfadhel M. SLC25A19-Related Thiamine Metabolism ...
    https://medlineplus.gov/genetics/condition/amish-lethal-microcephaly - Genetics
  8. Carnitine palmitoyltransferase II deficiency 
    ... heart beat (arrhythmia). Affected individuals also have low blood glucose (hypoglycemia) and a low level of ketones, ... JR, Dalton A, Leonard JV, Land JM, Andresen BS, Morris AA, Muntoni F, Turnbull D, Pourfarzam M, ...
    https://medlineplus.gov/...nitine-palmitoyltransferase-ii-deficiency - Genetics
  9. Idiopathic pulmonary fibrosis 
    ... and 70. Idiopathic pulmonary fibrosis belongs to a group of conditions called interstitial lung diseases (also known ... develop other serious lung conditions, including lung cancer, blood clots in the lungs (pulmonary emboli), pneumonia, or ...
    https://medlineplus.gov/.../condition/idiopathic-pulmonary-fibrosis - Genetics
  10. Motion sickness 
    ... enough.Motion sickness is more common in some groups of people than in others, for reasons that ... these conditions. People in some ethnic and geographic groups are more likely to report being susceptible to ...
    https://medlineplus.gov/genetics/condition/motion-sickness - Genetics
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