Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Smadar Abraham"'
Autor:
Or Steg Saban, Ben Pode-Shakked, Bassam Abu-Libdeh, Maya Granot, Galia Barkai, Yael Haberman, Inon Roterman, Avishay Lahad, Dror S. Shouval, Batia Weiss, Dina Marek-Yagel, Ortal Barel, Nurit Loberman-Nachum, Smadar Abraham, Raz Somech, David A. Weinstein, Yair Anikster
Publikováno v:
European journal of medical genetics. 65(6)
Avoidance of fasting and regular ingestion of uncooked-cornstarch have long been the mainstay dietary treatment of Glycogen Storage Disease type Ia (GSD-Ia). However, GSD-Ia patients who despite optimal dietary treatment show poor glycemic control an
Autor:
Eyal Kristal, Smadar Abraham, Ohad Wormser, Keren Porper, Orna Staretz-Chacham, Yair Anikster, Ilan Shelef, Ben Pode-Shakked
Publikováno v:
Nutrients
Volume 13
Issue 10
Nutrients, Vol 13, Iss 3523, p 3523 (2021)
Volume 13
Issue 10
Nutrients, Vol 13, Iss 3523, p 3523 (2021)
Background: Dihydrolipoamide dehydrogenase (DLD lipoamide dehydrogenase, the E3 subunit of the pyruvate dehydrogenase complex (PDHC)) is the third catalytic enzyme of the PDHC, which converts pyruvate to acetyl-CoA catalyzed with the introduction of
Autor:
Avraham Shaag, Suha Daas, Elon Pras, Ben Pode-Shakked, Smadar Abraham, Talya Saraf-Levy, Naomi Pode-Shakked, Shlomo Almashanu, Yuval Landau, Stanley H Korman, Haike Reznik-Wolf, Katya Kneller, Asaf Vivante, Yair Anikster, Igor Ulanovsky
Publikováno v:
European Journal of Medical Genetics. 63:103901
Background Maple syrup urine disease is a rare autosomal-recessive aminoacidopathy, caused by deficient branched-chain 2-keto acid dehydrogenase (BCKD), with subsequent accumulation of branched-chain amino acids (BCAAs): leucine, isoleucine and valin
Autor:
Smadar Abraham, Ben Pode-Shakked, Alon Harmelin, Noa Stettner, Yair Anikster, Gerard Schwartz, Ori Brenner, Lilach Shemer-Meiri
Publikováno v:
Molecular Genetics and Metabolism. 110:S66-S70
Introduction Phenylalanine (Phe) deficiency and its clinical manifestations have been previously described mostly as sporadic case reports dating back to the 1960's and 1970's. In these reports, low plasma Phe levels were associated with listlessness