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A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function.
Blood. 2008 Sep 1;112(5):2055-61. doi: 10.1182/blood-2008-04-150276. Epub 2008 Jun 17.
Blood. 2008.
PMID: 18559978
Free article.
Neurological manifestations of folate transport defect: case report and review of the literature.
Sofer Y, Harel L, Sharkia M, Amir J, Schoenfeld T, Straussberg R.
Sofer Y, et al. Among authors: sharkia m.
J Child Neurol. 2007 Jun;22(6):783-6. doi: 10.1177/0883073807304004.
J Child Neurol. 2007.
PMID: 17641272
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Thyroid function from birth to adolescence in Prader-Willi syndrome.
Sharkia M, Michaud S, Berthier MT, Giguère Y, Stewart L, Deladoëy J, Deal C, Van Vliet G, Chanoine JP.
Sharkia M, et al.
J Pediatr. 2013 Sep;163(3):800-5. doi: 10.1016/j.jpeds.2013.03.058. Epub 2013 Apr 25.
J Pediatr. 2013.
PMID: 23623517
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Serum transaminases as a prognostic factor in children post cardiac surgery.
Shteyer E, Yatsiv I, Sharkia M, Milgarter E, Granot E.
Shteyer E, et al. Among authors: sharkia m.
Pediatr Int. 2011 Oct;53(5):725-728. doi: 10.1111/j.1442-200X.2011.03356.x.
Pediatr Int. 2011.
PMID: 21410598
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Pancreatitis following hepatitis A vaccination.
Haviv YS, Sharkia M, Galun E, Safadi R.
Haviv YS, et al. Among authors: sharkia m.
Eur J Med Res. 2000 May 23;5(5):229-30.
Eur J Med Res. 2000.
PMID: 10806126
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Hypoglycemia in patients with renal failure.
Haviv YS, Sharkia M, Safadi R.
Haviv YS, et al. Among authors: sharkia m.
Ren Fail. 2000 Mar;22(2):219-23. doi: 10.1081/jdi-100100866.
Ren Fail. 2000.
PMID: 10803766
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