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The Niikawa‐Kuroki (Kabuki make‐up) syndrome in a Moslem Arab child

Clinical genetics, 1990-11, Vol.38 (5), p.378-381

1990

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Evidence that Griscelli Syndrome with Neurological Involvement Is Caused by Mutations in RAB27A, Not MYO5A

American journal of human genetics, 2002-08, Vol.71 (2), p.407-414

2002

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Familial absence of the trapezius muscle with associated shoulder girdle abnormalities

Clinical genetics, 1987-09, Vol.32 (3), p.145-147

1987

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Hepatitis A associated with other focal infections

The Israel Medical Association journal, 2000-08, Vol.2 (8), p.598-600

2000

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Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 16 non-Japanese cases

Clinical dysmorphology, 1992-04, Vol.1 (2), p.63-78

1992

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Intestinal Protein Loss and Hypoalbuminemia in Children with Pneumonia

Journal of pediatric gastroenterology and nutrition, 2003-08, Vol.37 (2), p.120-123

2003

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Ultrastructural abnormalities of the liver in total lipodystrophy

Archives of pathology & laboratory medicine (1976), 1987-02, Vol.111 (2), p.197

1987

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Sweet syndrome in early childhood

European journal of pediatrics, 1986-09, Vol.145 (4), p.303-305

1986

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Prostaglandins in Small Intestinal Mucosa of Children with Celiac Disease

Journal of pediatric gastroenterology and nutrition, 1984-11, Vol.3 (5), p.672-675

1984

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Rise of prostanoids in rat small intestinal mucosa following intestinal protein hypersensitivity

Pediatric research, 1987-04, Vol.21 (4), p.414-416

1987

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Impaired kinetic properties of hypoxanthine-guanine phosphoribosyl transferase as a cause of uric acid nephropathy in early infancy

European journal of pediatrics, 1987-11, Vol.146 (6), p.595-597

1987

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Near normalization of metabolic abnormalities by prolonged CSII in a girl with congenital lipodystrophy

Diabetes care, 1987-03, Vol.10 (2), p.257

1987

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A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter

Journal of medical genetics, 1984-12, Vol.21 (6), p.454-459

1984

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Neurological Dysfunction as a Presentation of Intussusception in an Infant

Journal of clinical gastroenterology, 1986-10, Vol.8 (5), p.604-604

1986

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Chronic Pigmented Purpura: A Case Report of Schamberg's Disease

Clinical pediatrics, 1987-12, Vol.26 (12), p.657-658

1987

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Pancytopenia caused by iron-dextran

Archives of disease in childhood, 1986-02, Vol.61 (2), p.194-196

1986

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High-dose intravenous gammaglobulin in the treatment of immune thrombocytopenic purpura

הרפואה, 1985-02, Vol.108 (3), p.149

1985

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Acute hydrops of the gallbladder in a child

Pediatric surgery international, 1988-05, Vol.3 (4), p.285-287

1988

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URTICARIA IN PATIENTS WITH HEPATITIS A VIRUS INFECTION

The Pediatric infectious disease journal, 1991-09, Vol.10 (9), p.702-702

1991

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Familial variant of maxillonasal dysplasia?

Journal of craniofacial genetics and developmental biology, 1986, Vol.6 (3), p.331

1986

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Shwachman-Diamond syndrome

הרפואה, 1983-09, Vol.105 (5-6), p.114

1983

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Cardio‐facio cutaneous syndrome: neurological manifestations

Clinical genetics, 1990-11, Vol.38 (5), p.382-386

1990

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Familial occurrence of the Freeman-Sheldon syndrome: cranio-carpotarsal dysplasia

Pediatrics (Evanston), 1971-06, Vol.47 (6), p.1064

1971

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Cardiomyopathy in lipodystrophy and the specificity spillover hypothesis

Israel journal of medical sciences, 1993-01, Vol.29 (1), p.50

1993

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Bloody Diarrhea—A Possible Complication of Sulfasalazine Transferred Through Human Breast Milk

Journal of pediatric gastroenterology and nutrition, 1986-03, Vol.5 (2), p.316-317

1986

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The Niikawa‐Kuroki (Kabuki make‐up) syndrome in a Moslem Arab child

Evidence that Griscelli Syndrome with Neurological Involvement Is Caused by Mutations in RAB27A, Not MYO5A

Familial absence of the trapezius muscle with associated shoulder girdle abnormalities

Hepatitis A associated with other focal infections

Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 16 non-Japanese cases

Intestinal Protein Loss and Hypoalbuminemia in Children with Pneumonia

Ultrastructural abnormalities of the liver in total lipodystrophy

Sweet syndrome in early childhood

Prostaglandins in Small Intestinal Mucosa of Children with Celiac Disease

Rise of prostanoids in rat small intestinal mucosa following intestinal protein hypersensitivity

Impaired kinetic properties of hypoxanthine-guanine phosphoribosyl transferase as a cause of uric acid nephropathy in early infancy

Near normalization of metabolic abnormalities by prolonged CSII in a girl with congenital lipodystrophy

A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter

Neurological Dysfunction as a Presentation of Intussusception in an Infant

Chronic Pigmented Purpura: A Case Report of Schamberg's Disease

Pancytopenia caused by iron-dextran

High-dose intravenous gammaglobulin in the treatment of immune thrombocytopenic purpura

Acute hydrops of the gallbladder in a child

URTICARIA IN PATIENTS WITH HEPATITIS A VIRUS INFECTION

Familial variant of maxillonasal dysplasia?

Shwachman-Diamond syndrome

Cardio‐facio cutaneous syndrome: neurological manifestations

Familial occurrence of the Freeman-Sheldon syndrome: cranio-carpotarsal dysplasia

Cardiomyopathy in lipodystrophy and the specificity spillover hypothesis

Bloody Diarrhea—A Possible Complication of Sulfasalazine Transferred Through Human Breast Milk

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