Sakati NA - Search Results

1

Genetic linkage studies of X-linked hypophosphataemic rickets in a Saudi Arabian family.

Thakker RV, Farmery MR, Sakati NA, Milner RD. Thakker RV, et al. Among authors: sakati na. Clin Endocrinol (Oxf). 1992 Oct;37(4):338-43. doi: 10.1111/j.1365-2265.1992.tb02335.x. Clin Endocrinol (Oxf). 1992. PMID: 1483289

2

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.

3

A novel mutation in the deoxyribonucleic acid-binding domain of the vitamin D receptor causes hereditary 1,25-dihydroxyvitamin D-resistant rickets.

Lin NU, Malloy PJ, Sakati N, al-Ashwal A, Feldman D. Lin NU, et al. J Clin Endocrinol Metab. 1996 Jul;81(7):2564-9. doi: 10.1210/jcem.81.7.8675579. J Clin Endocrinol Metab. 1996. PMID: 8675579

4

X-linked adrenoleukodystrophy. The Saudi experience.

Al-Essa MA, Sakati NA, Bakheet SM, Patay ZJ, Dabbagh O, Chaves-Carbello E, Ozand PT. Al-Essa MA, et al. Among authors: sakati na. Saudi Med J. 2000 Jan;21(1):61-71. Saudi Med J. 2000. PMID: 11533753

5

Unknown dysmorphic syndromes and development delay in Saudi Arabia.

Nester MJ, Sakati N, Greer W. Nester MJ, et al. J Child Neurol. 1992 Apr;7 Suppl:S64-8. doi: 10.1177/08830738920070010911. J Child Neurol. 1992. PMID: 1375238

6

Cystic fibrosis in Saudi Arabia.

Nazer H, Riff E, Sakati N, Mathew R, Majeed-Saidan MA, Harfi H. Nazer H, et al. Eur J Pediatr. 1989 Jan;148(4):330-2. doi: 10.1007/BF00444127. Eur J Pediatr. 1989. PMID: 2785036

7

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

Al-Ashwal AA, Shabib SM, Sakati NA, Attia NA. Al-Ashwal AA, et al. Among authors: sakati na. Saudi Med J. 2003 Oct;24(10):1113-5. Saudi Med J. 2003. PMID: 14578980

8

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

Sanjad SA, Kaddoura RE, Nazer HM, Akhtar M, Sakati NA. Sanjad SA, et al. Among authors: sakati na. Am J Dis Child. 1993 Sep;147(9):957-9. doi: 10.1001/archpedi.1993.02160330047016. Am J Dis Child. 1993. PMID: 8362811

9

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

Kelly TE, Blanton S, Saif R, Sanjad SA, Sakati NA. Kelly TE, et al. Among authors: sakati na. J Med Genet. 2000 Jan;37(1):63-4. doi: 10.1136/jmg.37.1.63. J Med Genet. 2000. PMID: 10691411 Free PMC article. No abstract available.

10

Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiency.

Al-Jishi E, Meyer BF, Rashed MS, Al-Essa M, Al-Hamed MH, Sakati N, Sanjad S, Ozand PT, Kambouris M. Al-Jishi E, et al. Clin Genet. 1999 Jun;55(6):444-9. doi: 10.1034/j.1399-0004.1999.550608.x. Clin Genet. 1999. PMID: 10450861

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