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Shimon Moses

Research Profile

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Publications

TOP 3
Isack Gabizon; Vladimir Khalameizer; Shimon W Moses; Victor Novack; Arthur Shiyovich; Chaim Yosefy; Amos Katz
Impact of descent and stay at a Dead Sea resort (low altitude) on patients with systolic congestive heart failure and an implantable cardioverter defibrillator.
Marco Harari; Lena Novack; Joachim Barth; Michael David; Michael Friger; Shimon W Moses
The percentage of patients achieving PASI 75 after 1 month and remission time after climatotherapy at the Dead Sea.
Shimon W Moses; Michael David; Ehud Goldhammer; Asher Tal; Shaul Sukenik
The Dead Sea, a unique natural health resort.

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All Publications

2011: Isack Gabizon; Vladimir Khalameizer; Shimon W Moses; Victor Novack; Arthur Shiyovich; Chaim Yosefy; Amos Katz
Impact of descent and stay at a Dead Sea resort (low altitude) on patients with systolic congestive heart failure and an implantable cardioverter defibrillator.
The Israel Medical Association journal : IMAJ 2011;13(7):402-7.
2007: Marco Harari; Lena Novack; Joachim Barth; Michael David; Michael Friger; Shimon W Moses
The percentage of patients achieving PASI 75 after 1 month and remission time after climatotherapy at the Dead Sea.
International journal of dermatology 2007;46(10):1087-91.
2006: Shimon W Moses; Michael David; Ehud Goldhammer; Asher Tal; Shaul Sukenik
The Dead Sea, a unique natural health resort.
The Israel Medical Association journal : IMAJ 2006;8(7):483-8.
2004: D Galron; Ohad Birk; A Kazanovitz; Shimon W Moses; Eli Hershkovitz
Carnitine-acylcarnitine translocase deficiency: identification of a novel molecular defect in a Bedouin patient.
Journal of inherited metabolic disease 2004;27(2):267-73.
2003: Barbara Burwinkel; Bin Hu; Anja Schroers; Paula R Clemens; Shimon W Moses; Yoon S Shin; Dieter Pongratz; Matthias Vorgerd; Manfred W Kilimann
Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of cases.
European journal of human genetics : EJHG 2003;11(7):516-26.
2002: Shimon W Moses
Historical highlights and unsolved problems in glycogen storage disease type 1.
European journal of pediatrics 2002;161 Suppl 1():S2-9.
2002: Shimon W Moses; Ruti Parvari
The variable presentations of glycogen storage disease type IV: a review of clinical, enzymatic and molecular studies.
Current molecular medicine 2002;2(2):177-88.
2001: Zamir Shorer; Shimon W Moses; Eli Hershkovitz; Vered Pinsk; Jaime Levy
Neurophysiologic studies in congenital insensitivity to pain with anhidrosis.
Pediatric neurology 2001;25(5):397-400.
1999: Ruti Parvari; J Isam; Shimon W Moses
Glycogen storage disease type 1a in three siblings with the G270V mutation.
Journal of inherited metabolic disease 1999;22(2):149-54.
1999: Hisayuki Hiraiwa; Chi-Jiunn Pan; B Lin; Shimon W Moses; Janice Yang Chou
Inactivation of the glucose 6-phosphate transporter causes glycogen storage disease type 1b.
The Journal of biological chemistry 1999;274(9):5532-6.
1998: Ruti Parvari; J Shen; Eli Hershkovitz; Y T Chen; Shimon W Moses
Two new mutations in the 3' coding region of the glycogen debranching enzyme in a glycogen storage disease type IIIa Ashkenazi Jewish patient.
Journal of inherited metabolic disease 1998;21(2):141-8.
1998: Barbara Burwinkel; H D Bakker; E Herschkovitz; Shimon W Moses; Yoon S Shin; Manfred W Kilimann
Mutations in the liver glycogen phosphorylase gene (PYGL) underlying glycogenosis type VI.
American journal of human genetics 1998;62(4):785-91.
1998: Borhane Annabi; Hisayuki Hiraiwa; Brian C Mansfield; KJ Lei; T Ubagai; Mihael H Polymeropoulos; Shimon W Moses; Ruti Parvari; Eli Hershkovitz; H Mandel; M Fryman; Janice Yang Chou
The gene for glycogen-storage disease type 1b maps to chromosome 11q23.
American journal of human genetics 1998;62(2):400-5.
1997: Barbara Burwinkel; Shimon W Moses; Manfred W Kilimann
Phosphorylase-kinase-deficient liver glycogenosis with an unusual biochemical phenotype in blood cells associated with a missense mutation in the beta subunit gene (PHKB).
Human genetics 1997;101(2):170-4.
1997: Ruti Parvari; KJ Lei; N Bashan; Eli Hershkovitz; Stanley H Korman; Varda Barash; Tally Lerman-Sagie; H Mandel; Janice Yang Chou; Shimon W Moses
Glycogen storage disease type 1a in Israel: biochemical, clinical, and mutational studies.
American journal of medical genetics 1997;72(3):286-90.
1994: J Levy; M T Abu-Ras; T Berenstein; Ruth Potashnik; I Meisner; Shimon W Moses; Nava Bashan
Postnatal regression of glucose transport in a patient with glycogen storage disease type 1b.
Journal of inherited metabolic disease 1994;17(1):16-22.
1993: Nava Bashan; Ruth Potashnik; A Peist; N Peleg; A Moran; Shimon W Moses
Deficient glucose phosphorylation as a possible common denominator and its relation to abnormal leucocyte function, in glycogen storage disease 1b patients.
European journal of pediatrics 1993;152 Suppl 1():S44-8.
1991: Shimon W Moses; Nava Bashan; B F Flasterstein; A Rachmel; A Gutman
Fructose-1,6-diphosphatase deficiency in Israel.
Israel journal of medical sciences 1991;27(1):1-4.
1990: Shimon W Moses
Pathophysiology and dietary treatment of the glycogen storage diseases.
Journal of pediatric gastroenterology and nutrition 1990;11(2):155-74.
1990: Ruth Potashnik; A Moran; Shimon W Moses; N Peleg; Nava Bashan
Hexose uptake and transport in polymorphonuclear leukocytes from patients with glycogen storage disease Ib.
Pediatric research 1990;28(1):19-23.
1990: Nava Bashan; Ruth Potashnik; N Peleg; A Moran; Shimon W Moses
Uptake and transport of hexoses into polymorphonuclear leukocytes of patients with glycogen storage disease type 1b.
Journal of inherited metabolic disease 1990;13(3):252-4.
1989: Shimon W Moses; K L Wanderman; A Myroz; M Frydman
Cardiac involvement in glycogen storage disease type III.
European journal of pediatrics 1989;148(8):764-6.
1989: A Singer; Moshe Phillip; D Hermoni; M Abelson; Shimon W Moses
Correlation between C-reactive protein and throat culture results in patients with pharyngitis.
Israel journal of medical sciences 1989;25(4):235-6.
1989: Shimon W Moses
Muscle glycogen phosphorylase deficiency.
Israel journal of medical sciences 1989;25(2):61-3.
1989: Shimon W Moses; M Aviram; R Geiger; R Berger; P C Smit
3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency.
Journal of inherited metabolic disease 1989;12(3):341-2.
1989: Nava Bashan; Ruth Potashnik; M Phillip; Y S Shin; Shimon W Moses
A method for the diagnosis of glycogen storage disease type Ib using polymorphonuclear leukocytes.
Journal of inherited metabolic disease 1989;12 Suppl 2():346-8.
1989: Shimon W Moses; Nava Bashan
Genetic aspects of muscle glycogenosis.
Progress in clinical and biological research 1989;306():149-61.
1988: Nava Bashan; Y Hagai; Ruth Potashnik; Shimon W Moses
Impaired carbohydrate metabolism of polymorphonuclear leukocytes in glycogen storage disease Ib.
The Journal of clinical investigation 1988;81(5):1317-22.
1988: Nava Bashan; Ruth Potashnik; V Barash; A Gutman; Shimon W Moses
Glycogen storage disease type II in Israel.
Israel journal of medical sciences 1988;24(4-5):224-7.
1988: Nava Bashan; N Peleg; Shimon W Moses
Attempts to predict the hemolytic potential of drugs in glucose-6-phosphate dehydrogenase deficiency of the Mediterranean type by an in vitro test.
Israel journal of medical sciences 1988;24(1):61-4.
1987: Shimon W Moses; M Phillip; Nava Bashan
[Nutritional therapy of glycogen storage disease types I and III].
Harefuah 1987;113(5-6):135-7.
1987: Moshe Phillip; N Bashan; C P Smith; Shimon W Moses
An algorithmic approach to diagnosis of hypoglycemia.
The Journal of pediatrics 1987;110(3):387-90.
1987: J M Abarbanel; Ruth Potashnik; S Frisher; Shimon W Moses; A Osimani; Yuval Herishanu
Myophosphorylase deficiency: the course of an unusual congenital myopathy.
Neurology 1987;37(2):316-8.
1987: Nava Bashan; Ruth Potashnik; T Ehrlich; Shimon W Moses
Phosphorylase kinase in leukocytes and erythrocytes of a patient with glycogen storage disease type IX.
Journal of inherited metabolic disease 1987;10(2):119-27.
1987: Nava Bashan; Ruth Potashnik; Y Hagay; Shimon W Moses
Impaired glucose transport in polymorphonuclear leukocytes in glycogen storage disease Ib.
Journal of inherited metabolic disease 1987;10(3):234-41.
1986: J M Abarbanel; Nava Bashan; Ruth Potashnik; A Osimani; Shimon W Moses; Yuval Herishanu
Adult muscle phosphorylase "b" kinase deficiency.
Neurology 1986;36(4):560-2.
1986: Shimon W Moses; N Gadoth; Nava Bashan; E Ben-David; A Slonim; K L Wanderman
Neuromuscular involvement in glycogen storage disease type III.
Acta paediatrica Scandinavica 1986;75(2):289-96.
1981: Nava Bashan; THEODORE C IANCU; A Lerner; D Fraser; Ruth Potashnik; Shimon W Moses
Glycogenosis due to liver and muscle phosphorylase kinase deficiency.
Pediatric research 1981;15(4 Pt 1):299-303.