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Hepatology (Baltimore, Md.)|June 30, 2001
Navajo neurohepatopathy: a mitochondrial DNA depletion syndrome?T H Vu, K Tanji, S A Holve, et al.
British Journal of Haematology|July 11, 2000
Fatal cold anti-i autoimmune haemolytic anaemia complicating hairy cell leukaemiaC J Mainwaring, R Walewska, J Snowden, et al.
British Journal of Haematology|November 1, 1995
The glycosylation of red cell autoantibodies affects their functional activity in vitroA G Hadley, B Zupanska, B M Kumpel, et al.
Pediatric Transplantation|March 25, 2005
Amylopectinosis disease isolated to the heart with normal glycogen branching enzyme activity and gene sequenceB B Das, M R Narkewicz, R J Sokol, et al.
American Journal of Diseases of Children (1960)|December 1, 1985
Frequency and clinical progression of the vitamin E deficiency neurologic disorder in children with prolonged neonatal cholestasisR J Sokol, M A Guggenheim, J E Heubi, et al.
American Journal of Obstetrics and Gynecology|April 1, 1995
MOMs (multiples of the median) and DADs (discriminant aneuploidy detection): improved specificity and cost-effectiveness of biochemical screening for aneuploidy with DADsM I Evans, L Chik, J E O'Brien, et al.
Gynecologic Oncology|February 1, 1991
A phase II evaluation of cisplatin, bleomycin, and mitomycin-C in patients with recurrent squamous cell carcinoma of the cervixM S Hoffman, J J Kavanagh, W S Roberts, et al.
Gastroenterology|June 1, 1993
Multicenter trial of d-alpha-tocopheryl polyethylene glycol 1000 succinate for treatment of vitamin E deficiency in children with chronic cholestasisR J Sokol, N Butler-Simon, C Conner, et al.
Surgical Endoscopy|January 30, 2020
Health benefits and risks during 10 years after Roux-en-Y gastric bypassM Chahal-Kummen, O B K Salte, S Hewitt, et al.
The Journal of Clinical Investigation|November 5, 1998
Identification of a new inborn error in bile acid synthesis: mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver diseaseK D Setchell, M Schwarz, N C O'Connell, et al.
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