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The variable presentations of glycogen storage disease type IV: a review of clinical, enzymatic and molecular studies

Current molecular medicine, 2002-03, Vol.2 (2), p.177-188

2002

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The percentage of patients achieving PASI 75 after 1 month and remission time after climatotherapy at the Dead Sea

International journal of dermatology, 2007-10, Vol.46 (10), p.1087-1091

2007

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Historical highlights and unsolved problems in glycogen storage disease type 1

European journal of pediatrics, 2002-10, Vol.161 Suppl 1 (1), p.S2-S9

Moses, Shimon W

2002

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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, 2011-07, Vol.13 (7), p.402-407

2011

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Historical highlights and unsolved problems in glycogen storage disease type 1

European journal of pediatrics, 2002-01, Vol.161, p.S2-S9

Moses, Shimon

2002

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The Dead Sea, a unique natural health resort

The Israel Medical Association journal, 2006-07, Vol.8 (7), p.483-488

2006

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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, 2003-07, Vol.11 (7), p.516-526

2003

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Inactivation of the Glucose 6-Phosphate Transporter Causes Glycogen Storage Disease Type 1b

The Journal of biological chemistry, 1999-02, Vol.274 (9), p.5532-5536

1999

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Neurophysiologic studies in congenital insensitivity to pain with anhidrosis

Pediatric neurology, 2001-11, Vol.25 (5), p.397-400

2001

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A Single-Base Deletion in the 3'-Coding Region of Glycogen-Debranching Enzyme Is Prevalent in Glycogen Storage Disease Type IIIA in a Population of North African Jewish Patients

European journal of human genetics : EJHG, 1997-09, Vol.5 (5), p.266-270

1997

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Efectos saludables de la Climatoterapia del Mar Muerto en pacientes con enfermedades cardíacas y pulmonares

Anales de hidrología médica, 2012-07, Vol.5 (1)

W. Moses, Shimon

2012

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Glycogen storage disease type III in Israel: presentation and long-term outcome

Pediatric endocrinology reviews : PER, 2014-03, Vol.11 (3), p.318

2014

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The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome

Human genetics, 2002, Vol.110 (1), p.21-29

2002

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A Recessive Contiguous Gene Deletion of Chromosome 2p16 Associated with Cystinuria and a Mitochondrial Disease

American journal of human genetics, 2001-10, Vol.69 (4), p.869-875

2001

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Impaired glucose homeostasis, neutrophil trafficking and function in mice lacking the glucose-6-phosphate transporter

Human molecular genetics, 2003-10, Vol.12 (19), p.2547-2558

2003

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Horizon scanning in medical education: 2020 vision

The Israel Medical Association journal, 2001-06, Vol.3 (6), p.465-465

Moses, S

2001

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Hyperbaric oxygen at the Dead Sea

The Israel Medical Association journal, 2002-09, Vol.4 (9), p.745-746

Moses, Shimon

2002

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Granulocyte colony-stimulating factor in glycogen storage disease type 1b. Results of the European Study on Glycogen Storage Disease Type 1

European journal of pediatrics, 2002-10, Vol.161 Suppl 1 (1), p.S83-S87

2002

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Mutations in the Liver Glycogen Phosphorylase Gene ( PYGL) Underlying Glycogenosis Type VI (Hers Disease)

American journal of human genetics, 1998-04, Vol.62 (4), p.785-791

1998

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Dexamethasone and salbutamol in the treatment of acute wheezing in infants

Pediatrics (Evanston), 1983-01, Vol.71 (1), p.13-18

1983

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Consensus guidelines for management of glycogen storage disease type 1b - European Study on Glycogen Storage Disease Type 1

European journal of pediatrics, 2002-01, Vol.161, p.S120-S123

2002

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The Gene for Glycogen-Storage Disease Type 1b Maps to Chromosome 11q23

American journal of human genetics, 1998-02, Vol.62 (2), p.400-405

1998

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Consensus guidelines for management of glycogen storage disease type 1b - European Study on Glycogen Storage Disease Type 1

European journal of pediatrics, 2002-10, Vol.161 Suppl 1 (1), p.S120-S123

2002

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Pathophysiology and Dietary Treatment of the Glycogen Storage Diseases

Journal of pediatric gastroenterology and nutrition, 1990-08, Vol.11 (2), p.155-174

Moses, Shimon W.

1990

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Granulocyte colony-stimulating factor in glycogen storage disease type 1b. Results of the European Study on Glycogen Storage Disease Type 1

European journal of pediatrics, 2002-01, Vol.161, p.S83-S87

2002

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The variable presentations of glycogen storage disease type IV: a review of clinical, enzymatic and molecular studies

The percentage of patients achieving PASI 75 after 1 month and remission time after climatotherapy at the Dead Sea

Historical highlights and unsolved problems in glycogen storage disease type 1

Impact of descent and stay at a Dead Sea resort (low altitude) on patients with systolic congestive heart failure and an implantable cardioverter defibrillator

Historical highlights and unsolved problems in glycogen storage disease type 1

The Dead Sea, a unique natural health resort

Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of cases

Inactivation of the Glucose 6-Phosphate Transporter Causes Glycogen Storage Disease Type 1b

Neurophysiologic studies in congenital insensitivity to pain with anhidrosis

A Single-Base Deletion in the 3'-Coding Region of Glycogen-Debranching Enzyme Is Prevalent in Glycogen Storage Disease Type IIIA in a Population of North African Jewish Patients

Efectos saludables de la Climatoterapia del Mar Muerto en pacientes con enfermedades cardíacas y pulmonares

Glycogen storage disease type III in Israel: presentation and long-term outcome

The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome

A Recessive Contiguous Gene Deletion of Chromosome 2p16 Associated with Cystinuria and a Mitochondrial Disease

Impaired glucose homeostasis, neutrophil trafficking and function in mice lacking the glucose-6-phosphate transporter

Horizon scanning in medical education: 2020 vision

Hyperbaric oxygen at the Dead Sea

Granulocyte colony-stimulating factor in glycogen storage disease type 1b. Results of the European Study on Glycogen Storage Disease Type 1

Mutations in the Liver Glycogen Phosphorylase Gene ( PYGL) Underlying Glycogenosis Type VI (Hers Disease)

Dexamethasone and salbutamol in the treatment of acute wheezing in infants

Consensus guidelines for management of glycogen storage disease type 1b - European Study on Glycogen Storage Disease Type 1

The Gene for Glycogen-Storage Disease Type 1b Maps to Chromosome 11q23

Consensus guidelines for management of glycogen storage disease type 1b - European Study on Glycogen Storage Disease Type 1

Pathophysiology and Dietary Treatment of the Glycogen Storage Diseases

Granulocyte colony-stimulating factor in glycogen storage disease type 1b. Results of the European Study on Glycogen Storage Disease Type 1

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