Inclusion of joint laxity, recurrent patellar dislocation, and short distal ulnae as a feature of Van Den Ende-Gupta syndrome: a case report von Al-Qattan, Mohammad M, Andejani, Doaa F, Sakati, Nadia A, Ramzan, Khushnooda, Imtiaz, Faiqa

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Long-term outcome of genital reconstruction of Middle Eastern women with congenital adrenal hyperplasia von Seyam, Raouf, Bissada, Nabil, Abdul-Aaly, Mohamed, Sakati, Nadia, Al Taweel, Waleed, Alkhudair, Waleed

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Glycemic control and treatment satisfaction in Saudi diabetic children on insulin pump therapy von Bin-Abbas, Bassam S, Sakati, Nadia A, Al-Ashwal, Abdullah A

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Continuous subcutaneous insulin infusion in type 1 diabetic Saudi children : A comparison with conventional insulin therapy von BIN-ABBAS, Bassam S, SAKATI, Nadia A, RAEF, Hussein, AL-ASHWAL, Abdullah A

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Gender identity in congenital adrenal hyperplasia secondary to 11-hydroxylase deficiency von Bin-Abbas, Bassam S, Sakati, Nadia A, Al-Ashwal, Abdullah A

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Prevalence and characteristics of celiac disease in type I diabetes mellitus in Saudi Arabia von AL-ASHWAL, Abdullah A, SHABIB, Souheil M, SAKATI, Nadia A, ATTIA, Najya A

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Glycemic control and treatment satisfaction in Saudi diabetic children on insulin pump therapy von Bin-Abbas, Bassam S, Sakati, Nadia A, Al-Ashwal, Abdullah A

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Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase type II deficiency in 4 Saudi children. Long term follow up von BIN-ABBAS, Bassam S, SAKATI, Nadia A, AL-ASHWAL, Abdullah A

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Multiple daily insulin regimen using insulin glargine in type 1 diabetic Saudi children von BIN-ABBAS, Bassam S, AL-AGHA, Abdulmoein E, SAKATI, Nadia A, ABDULLAH A

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Diabetes mellitus and cystic fibrosis in 2 Saudi siblings von BANJAR, Hanaa H, SAKATI, Nadia A

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Radiological features of bisphosphonate therapy in children with osteogenesis imperfecta von BIN-ABBAS, Bassam S, AL-ASHWAL, Abdullah A, AL-ZAYED, Zayed S, SAKATI, Nadia A

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Persistent hyperinsulinemic hypoglycemia of infancy in 38 children von BIN-ABBAS, Bassam S, AL-MULHIM, Abdulmohsen N, SAKATI, Nadia A, AL-ASHWAL, Abdullah A

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The syndrome of septo-optic dysplasia in Saudi children von BIN-ABBAS, Bassam S, AL-ASHWAL, Abdullah A, AL-ALWAN, Ibrahim A, AL-QAHTANI, Mohammad H, AL-MUTAIR, Angham N, SAKATI, Nadia A

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Inborn Error of Vitamin B12 Metabolism: A Treatable Cause of Childhood Dementia/Paralysis von Al Essa, Mohammed, Sakati, Nadia A., Dabbagh, Omar, Joshi, Surrendra, Al Jishi, Emtethal A., Rashed, Mohamed S., Powe, John E., Ozand, Pinar T.

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Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome lq42-43 von KELLY, THADDEUS E, BLANTON, SUSAN, SAIF, RAMLA, SANJAD, SAMI A, SAKATI, NADIA A

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X-linked adrenoleukodystrophy : The Saudi experience von AL-ESSA, M. A, SAKATI, N. A, BAKHEET, S. M, PATAY, Z. J, DABBAGH, O, CHAVES-CARBALLO, E, OZAND, P. T

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Leber's Congenital Amaurosis Associated with Familial Juvenile Nephronophthisis and Cone-Shaped Epiphyses of the Hands (the Saldino-Mainzer Syndrome) von Ellis, Don S., Heckenlively, John R., Martin, Christina L., Lachman, Ralph S., Sakati, Nadia A., Rimoin, David L.

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Crossed ectopia of a solitary kidney associated with anal atresia von Bissada, N K, Cumming, W A, Sakati, N A, Hanash, K A, Ratcliffe, J W

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Concurrence of robinow syndrome and Crigler-Najar syndrome in two offspring of first cousins von Nazer, Hisham, Gunasekaran, Thirumazhisai S., Sakati, Nadia A., Nyhan, William L.

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Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss von Ramzan, Khushnooda, Al-Numair, Nouf S, Al-Ageel, Sarah, Elbaik, Lina, Sakati, Nadia, Al-Hazzaa, Selwa A F, Al-Owain, Mohammed, Imtiaz, Faiqa

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