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Familial Mediterranean fever: clinical and genetic characterization in a mixed pediatric population of Jewish and Arab patients

Pediatrics (Evanston), 1999-05, Vol.103 (5), p.e70-e70

1999

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Developmental dysplasia of the hip: a new approach to incidence

Pediatrics (Evanston), 1999-01, Vol.103 (1), p.93-99

1999

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Progressive Familial Intrahepatic Cholestasis Among the Arab Population in Israel

Journal of pediatric gastroenterology and nutrition, 1997-05, Vol.24 (5), p.548-554

1997

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Coexistence of Hereditary Homocystinuria and Factor V Leiden — Effect on Thrombosis

The New England journal of medicine, 1996-03, Vol.334 (12), p.763-768

1996

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Plasmalogen Phospholipids Are Involved in HDL-Mediated Cholesterol Efflux: Insights from Investigations with Plasmalogen-Deficient Cells

Biochemical and biophysical research communications, 1998-09, Vol.250 (2), p.369-373

1998

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Insulin in human milk and the prevention of type 1 diabetes

Pediatric diabetes, 2001-12, Vol.2 (4), p.175-177

2001

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Familial Mediterranean fever: high gene frequency and heterogeneous disease among an Israeli-Arab population

Journal of rheumatology, 2000-06, Vol.27 (6), p.1492

2000

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New supplements to infant formulas

Pediatric endocrinology reviews : PER, 2004-12, Vol.2 (2), p.216

2004

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Bacterial meningitis: effect of antibiotic treatment on cerebrospinal fluid

American journal of clinical pathology, 1983-09, Vol.80 (3), p.386-387

1983

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Progressive diaphyseal dysplasia: genetics and clinical and radiologic manifestations

Pediatrics (Evanston), 1984-09, Vol.74 (3), p.399-405

1984

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Influence of oral insulin supplementation on carbohydrate, lipid and protein metabolism in weaned Balb/c mice

Journal of Pediatric Endocrinology and Metabolism, 2003-03, Vol.16 (3), p.431

2003

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MPGN type I induced by granulocyte colony stimulating factor

Pediatric nephrology (Berlin, West), 2002-05, Vol.17 (5), p.370-372

2002

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“Infantile Colic” as the Sole Manifestation of Gastroesophageal Reflux

Journal of pediatric gastroenterology and nutrition, 1997-02, Vol.24 (2), p.231-233

1997

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Insulin in human milk and the prevention of type 1 diabetes: Insulin in human milk and type 1 diabetes

Pediatric diabetes, 2001-12, Vol.2 (4), p.175-177

2001

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A novel thermoregulatory system maintains perioperative normothermia in children undergoing elective surgery

Pediatric anesthesia, 2001-09, Vol.11 (5), p.555-560

2001

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Duration of methotrexate treatment until partial and total remission of refractory juvenile rheumatoid arthritis

Annals of the rheumatic diseases, 1998-03, Vol.57 (3), p.174-175

1998

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“Infantile Colic” as the Sole Manifestation of Gastroesophageal Reflux

Journal of pediatric gastroenterology and nutrition, 1997-02, Vol.24 (2), p.231-233

1997

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Retention of drugs in venous access port chamber: A note of caution

BMJ. British medical journal (International ed.), 1996-02, Vol.312 (7029), p.496

International edition, 1996

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Frequency of change of ventilator circuit in premature infants: Impact on ventilator-associated pneumonia

Pediatric critical care medicine, 2001-04, Vol.2 (2), p.127-132

2001

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Thrombophilia, Homocystinuria, and Mutation of the Factor V Gene

The New England journal of medicine, 1996-07, Vol.335 (4), p.289-290

1996

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Renal and Hematological Complications in Long-Term Treatment with Granulocyte Colony-Stimulating Factor 779

Pediatric research, 1998-04, Vol.43, p.135-135

1998

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Effect of Iron Deficiency on Small Intestinal Permeability in Infants and Young Children

Journal of pediatric gastroenterology and nutrition, 1992-01, Vol.14 (1), p.17-20

1992

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Impaired Cholesterol Synthesis Rate in Fibroblasts and Reduced Cellular Uptake of LDLs Derived from Peroxisome‐deficient Patients Cause Cellular Cholesterol Deficiency in Peroxisome‐deficient Fibroblastsa

Annals of the New York Academy of Sciences, 1996-12, Vol.804 (1), p.752-755

1996

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Localization of a Gene for Molybdenum Cofactor Deficiency, on the Short Arm of Chromosome 6, by Homozygosity Mapping

American journal of human genetics, 1998-07, Vol.63 (1), p.148-154

1998

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Nonspecific Duodenitis: An Unusual Presentation

Journal of pediatric gastroenterology and nutrition, 1997-04, Vol.24 (4), p.434-438

1997

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Familial Mediterranean fever: clinical and genetic characterization in a mixed pediatric population of Jewish and Arab patients

Developmental dysplasia of the hip: a new approach to incidence

Progressive Familial Intrahepatic Cholestasis Among the Arab Population in Israel

Coexistence of Hereditary Homocystinuria and Factor V Leiden — Effect on Thrombosis

Plasmalogen Phospholipids Are Involved in HDL-Mediated Cholesterol Efflux: Insights from Investigations with Plasmalogen-Deficient Cells

Insulin in human milk and the prevention of type 1 diabetes

Familial Mediterranean fever: high gene frequency and heterogeneous disease among an Israeli-Arab population

New supplements to infant formulas

Bacterial meningitis: effect of antibiotic treatment on cerebrospinal fluid

Progressive diaphyseal dysplasia: genetics and clinical and radiologic manifestations

Influence of oral insulin supplementation on carbohydrate, lipid and protein metabolism in weaned Balb/c mice

MPGN type I induced by granulocyte colony stimulating factor

“Infantile Colic” as the Sole Manifestation of Gastroesophageal Reflux

Insulin in human milk and the prevention of type 1 diabetes: Insulin in human milk and type 1 diabetes

A novel thermoregulatory system maintains perioperative normothermia in children undergoing elective surgery

Duration of methotrexate treatment until partial and total remission of refractory juvenile rheumatoid arthritis

“Infantile Colic” as the Sole Manifestation of Gastroesophageal Reflux

Retention of drugs in venous access port chamber: A note of caution

Frequency of change of ventilator circuit in premature infants: Impact on ventilator-associated pneumonia

Thrombophilia, Homocystinuria, and Mutation of the Factor V Gene

Renal and Hematological Complications in Long-Term Treatment with Granulocyte Colony-Stimulating Factor 779

Effect of Iron Deficiency on Small Intestinal Permeability in Infants and Young Children

Impaired Cholesterol Synthesis Rate in Fibroblasts and Reduced Cellular Uptake of LDLs Derived from Peroxisome‐deficient Patients Cause Cellular Cholesterol Deficiency in Peroxisome‐deficient Fibroblastsa

Localization of a Gene for Molybdenum Cofactor Deficiency, on the Short Arm of Chromosome 6, by Homozygosity Mapping

Nonspecific Duodenitis: An Unusual Presentation

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