Authors:
ALESSA M
SAKATI NA
DABBAGH O
JOSHI S
ALJISHI E
RASHED MS
POWE JE
OZAND PT
Citation: M. Alessa et al., INBORN ERROR OF VITAMIN-B-12 METABOLISM - A TREATABLE CAUSE OF CHILDHOOD DEMENTIA PARALYSIS/, Journal of child neurology, 13(5), 1998, pp. 239-243
Authors:
ALHAZZAA SAF
OZAND PT
SAKATI NA
MAUMENEE IH
Citation: Saf. Alhazzaa et al., CONVOLUTED RETINAL VEINS AS A SIGN OF SHORT-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY, Investigative ophthalmology & visual science, 36(4), 1995, pp. 620-620
Authors:
FRAYHA HH
SHAHEEN H
GANELIN RS
KATTAN HA
TUFENKEJI HT
KROTZER S
BARRETTO L
SCHAART W
ALSABBAN EA
SAKATI NA
Citation: Hh. Frayha et al., CLINICAL AND SEROLOGIC RESPONSES OF SAUDI CHILDREN TO HAEMOPHILUS-INFLUENZAE TYPE-B CAPSULAR POLYSACCHARIDE DIPHTHERIA TOXOID CONJUGATE VACCINE, Annals of saudi medicine, 13(3), 1993, pp. 215-221
Authors:
PHILLIPS JA
COGAN JD
MILLENDAVIS S
MILNER RDG
SAKATI NA
SCHENKMAN SS
BUNDEY SE
Citation: Ja. Phillips et al., MOLECULAR-BASIS OF AUTOSOMAL RECESSIVE AND AUTOSOMAL-DOMINANT INHERITANCE OF FAMILIAL GH DEFICIENCY, American journal of human genetics, 53(3), 1993, pp. 6-6
Authors:
SANJAD SA
KADDOURA RE
NAZER HM
AKHTAR M
SAKATI NA
Citation: Sa. Sanjad et al., FANCONIS-SYNDROME WITH HEPATORENAL GLYCOGENOSIS ASSOCIATED WITH PHOSPHORYLASE-B KINASE-DEFICIENCY, American journal of diseases of children [1960], 147(9), 1993, pp. 957-959