Sakati N - Search Results

1

Bone marrow transplantation for infantile malignant osteopetrosis.

Solh H, Da Cunha AM, Giri N, Padmos A, Spence D, Clink H, Ernst P, Sakati N. Solh H, et al. Among authors: sakati n. J Pediatr Hematol Oncol. 1995 Nov;17(4):350-5. doi: 10.1097/00043426-199511000-00013. J Pediatr Hematol Oncol. 1995. PMID: 7583393

2

Persistent hyperinsulinemic hypoglycemia of infancy: experience with 28 cases.

al-Rabeeah A, al-Ashwal A, al-Herbish A, al-Jurayyan N, Sakati N, Abobakr A. al-Rabeeah A, et al. Among authors: sakati n. J Pediatr Surg. 1995 Aug;30(8):1119-21. doi: 10.1016/0022-3468(95)90001-2. J Pediatr Surg. 1995. PMID: 7472962

3

Different faces of non-autoimmune diabetes of infancy.

Attia N, Zahrani A, Saif R, Kattan HA, Sakati N, Al Ashwal A, Tamborlane WV. Attia N, et al. Among authors: sakati n. Acta Paediatr. 1998 Jan;87(1):95-7. doi: 10.1080/08035259850157958. Acta Paediatr. 1998. PMID: 9510456

4

Endocrine sequelae of childhood craniopharyngioma.

Bin-Abbas B, Mawlawi H, Sakati N, Khafaja Y, Chaudhary MA, Al-Ashwal A. Bin-Abbas B, et al. Among authors: sakati n. J Pediatr Endocrinol Metab. 2001 Jul-Aug;14(7):869-74. doi: 10.1515/jpem.2001.14.7.869. J Pediatr Endocrinol Metab. 2001. PMID: 11515727

5

Pituitary gland enlargement in primary hypothyroidism: a report of 5 cases with follow-up data.

Ahmed M, Banna M, Sakati N, Woodhouse N. Ahmed M, et al. Among authors: sakati n. Horm Res. 1989;32(5-6):188-92. doi: 10.1159/000181287. Horm Res. 1989. PMID: 2634612

6

Radiological features of bisphosphonate therapy in children with osteogenesis imperfecta.

Bin-Abbas BS, Al-Ashwal AA, Al-Zayed ZS, Sakati NA. Bin-Abbas BS, et al. Saudi Med J. 2004 Nov;25(11):1772-3. Saudi Med J. 2004. PMID: 15573233 No abstract available.

7

Infantile systemic hyalinosis: a fatal disorder commonly diagnosed among Arabs.

Al-Mayouf SM, AlMehaidib A, Bahabri S, Shabib S, Sakati N, Teebi AS. Al-Mayouf SM, et al. Among authors: sakati n. Clin Exp Rheumatol. 2005 Sep-Oct;23(5):717-20. Clin Exp Rheumatol. 2005. PMID: 16173255

8

A recessive form of Marshall syndrome is caused by a mutation in the COL11A1 gene.

Khalifa O, Imtiaz F, Allam R, Al-Hassnan Z, Al-Hemidan A, Al-Mane K, Abuharb G, Balobaid A, Sakati N, Hyland J, Al-Owain M. Khalifa O, et al. Among authors: sakati n. J Med Genet. 2012 Apr;49(4):246-8. doi: 10.1136/jmedgenet-2012-100783. J Med Genet. 2012. PMID: 22499343 No abstract available.

9

A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features.

Sanjad SA, Sakati NA, Abu-Osba YK, Kaddoura R, Milner RD. Sanjad SA, et al. Among authors: sakati na. Arch Dis Child. 1991 Feb;66(2):193-6. doi: 10.1136/adc.66.2.193. Arch Dis Child. 1991. PMID: 2001103 Free PMC article.

10

Ethylmalonic aciduria: an organic acidemia with CNS involvement and vasculopathy.

Ozand PT, Rashed M, Millington DS, Sakati N, Hazzaa S, Rahbeeni Z, al Odaib A, Youssef N, Mazrou A, Gascon GG, et al. Ozand PT, et al. Among authors: sakati n. Brain Dev. 1994 Nov;16 Suppl:12-22. doi: 10.1016/0387-7604(94)90092-2. Brain Dev. 1994. PMID: 7726376

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