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Results: 5

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
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