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Inclusion of joint laxity, recurrent patellar dislocation, and short distal ulnae as a feature of Van Den Ende-Gupta syndrome: a case report

BMC medical genetics, 2018-01, Vol.19 (1), p.18-18, Article 18

2018

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Long-term outcome of genital reconstruction of Middle Eastern women with congenital adrenal hyperplasia

Urology annals, 2013-10, Vol.5 (4), p.277-282

2013

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Glycemic control and treatment satisfaction in Saudi diabetic children on insulin pump therapy

Annals of Saudi medicine, 2006-09, Vol.26 (5), p.405-405

2006

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Continuous subcutaneous insulin infusion in type 1 diabetic Saudi children. A comparison with conventional insulin therapy

Saudi medical journal, 2005-06, Vol.26 (6), p.918

2005

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Gender identity in congenital adrenal hyperplasia secondary to 11-hydroxylase deficiency

Annals of Saudi medicine, 2006-05, Vol.26 (3), p.239-241

2006

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Prevalence and characteristics of celiac disease in type I diabetes mellitus in Saudi Arabia

Saudi medical journal, 2003-10, Vol.24 (10), p.1113

2003

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Glycemic control and treatment satisfaction in Saudi diabetic children on insulin pump therapy

Annals of Saudi medicine, 2006-05, Vol.26 (3), p.247-248

2006

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Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase type II deficiency in 4 Saudi children. Long term follow up

Saudi medical journal, 2004-09, Vol.25 (9), p.1293

2004

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Multiple daily insulin regimen using insulin glargine in type 1 diabetic Saudi children

Saudi medical journal, 2006-02, Vol.27 (2), p.262

2006

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Diabetes mellitus and cystic fibrosis in 2 Saudi siblings

Saudi medical journal, 2002-12, Vol.23 (12), p.1541

2002

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Radiological features of bisphosphonate therapy in children with osteogenesis imperfecta

Saudi medical journal, 2004-11, Vol.25 (11), p.1772

2004

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Persistent hyperinsulinemic hypoglycemia of infancy in 38 children

Saudi medical journal, 2003-08, Vol.24 (8), p.890

2003

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The syndrome of septo-optic dysplasia in Saudi children

Saudi medical journal, 2004-11, Vol.25 (11), p.1675

2004

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Inborn Error of Vitamin B12 Metabolism: A Treatable Cause of Childhood Dementia/Paralysis

Journal of child neurology, 1998-05, Vol.13 (5), p.239-243

1998

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Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome lq42-43

Journal of medical genetics, 2000-01, Vol.37 (1), p.63-64

2000

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Fanconi's syndrome with hepatorenal glycogenosis associated with phosphorylase b kinase deficiency

American journal of diseases of children (1960), 1993-09, Vol.147 (9), p.957

1993

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X-linked adrenoleukodystrophy. The Saudi experience

Saudi medical journal, 2000-01, Vol.21 (1), p.61

2000

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Leber's Congenital Amaurosis Associated with Familial Juvenile Nephronophthisis and Cone-Shaped Epiphyses of the Hands (the Saldino-Mainzer Syndrome)

American journal of ophthalmology, 1984-02, Vol.97 (2), p.233-239

1984

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Clinical and Serologic Responses of Saudi Children to Hemophilus Influenzae Type B Capsular Polysaccharide Diphtheria Toxoid Conjugate Vaccine

Annals of Saudi medicine, 1993-05, Vol.13 (3), p.215-221

1993

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Johanson-Blizzard syndrome in a large inbred kindred with three involved members

Clinical genetics, 1978-11, Vol.14 (5), p.247-250

1978

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Crossed ectopia of a solitary kidney associated with anal atresia

Southern medical journal (Birmingham, Ala.), 1986-05, Vol.79 (5), p.648-649

1986

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Overwhelming Postsplenectomy Sepsis in Children: The King Faisal Specialist Hospital and Research Centre experience and review of the literature

Annals of Saudi medicine, 1982-01, Vol.2 (1), p.15-20

1982

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Concurrence of robinow syndrome and Crigler-Najar syndrome in two offspring of first cousins

American journal of medical genetics, 1990-12, Vol.37 (4), p.516-518

1990

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Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss

Genes, 2020-12, Vol.11 (12), p.1474

2020

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GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome

American journal of human genetics, 2017-05, Vol.100 (5), p.831-836

2017

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Inclusion of joint laxity, recurrent patellar dislocation, and short distal ulnae as a feature of Van Den Ende-Gupta syndrome: a case report

Long-term outcome of genital reconstruction of Middle Eastern women with congenital adrenal hyperplasia

Glycemic control and treatment satisfaction in Saudi diabetic children on insulin pump therapy

Continuous subcutaneous insulin infusion in type 1 diabetic Saudi children. A comparison with conventional insulin therapy

Gender identity in congenital adrenal hyperplasia secondary to 11-hydroxylase deficiency

Prevalence and characteristics of celiac disease in type I diabetes mellitus in Saudi Arabia

Glycemic control and treatment satisfaction in Saudi diabetic children on insulin pump therapy

Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase type II deficiency in 4 Saudi children. Long term follow up

Multiple daily insulin regimen using insulin glargine in type 1 diabetic Saudi children

Diabetes mellitus and cystic fibrosis in 2 Saudi siblings

Radiological features of bisphosphonate therapy in children with osteogenesis imperfecta

Persistent hyperinsulinemic hypoglycemia of infancy in 38 children

The syndrome of septo-optic dysplasia in Saudi children

Inborn Error of Vitamin B12 Metabolism: A Treatable Cause of Childhood Dementia/Paralysis

Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome lq42-43

Fanconi's syndrome with hepatorenal glycogenosis associated with phosphorylase b kinase deficiency

X-linked adrenoleukodystrophy. The Saudi experience

Leber's Congenital Amaurosis Associated with Familial Juvenile Nephronophthisis and Cone-Shaped Epiphyses of the Hands (the Saldino-Mainzer Syndrome)

Clinical and Serologic Responses of Saudi Children to Hemophilus Influenzae Type B Capsular Polysaccharide Diphtheria Toxoid Conjugate Vaccine

Johanson-Blizzard syndrome in a large inbred kindred with three involved members

Crossed ectopia of a solitary kidney associated with anal atresia

Overwhelming Postsplenectomy Sepsis in Children: The King Faisal Specialist Hospital and Research Centre experience and review of the literature

Concurrence of robinow syndrome and Crigler-Najar syndrome in two offspring of first cousins

Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss

GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome

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