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Results: 1-10 |
Results: 10
AN EPIDEMIOLOGIC, CLINICAL, AND THERAPEUTIC STUDY OF CHILDHOOD GUILLAIN-BARRE-SYNDROME IN KUWAIT - IS IT RELATED TO THE ORAL POLIO VACCINE
Authors: ISMAIL EAR SHABANI IS BADAWI M SANAA H MADI S ALTAWARI A NADI H ZAKI M ALSALEH Q
Citation: Ear. Ismail et al., AN EPIDEMIOLOGIC, CLINICAL, AND THERAPEUTIC STUDY OF CHILDHOOD GUILLAIN-BARRE-SYNDROME IN KUWAIT - IS IT RELATED TO THE ORAL POLIO VACCINE, Journal of child neurology, 13(10), 1998, pp. 488-492
BETA-THALASSEMIA MAJOR IN KUWAIT
Authors: ALFUZAE L ABOOLBACKER KC ALSALEH Q
Citation: L. Alfuzae et al., BETA-THALASSEMIA MAJOR IN KUWAIT, Journal of tropical pediatrics, 44(5), 1998, pp. 311-312
KENNY-CAFFEY-SYNDROME IS PART OF THE CATCH-22 HAPLOINSUFFICIENCY CLUSTER
Authors: SABRY MA ZAKI M HASSAN SJA RAMADAN DG RASOOL MAA ALAWADI SA ALSALEH Q
Citation: Ma. Sabry et al., KENNY-CAFFEY-SYNDROME IS PART OF THE CATCH-22 HAPLOINSUFFICIENCY CLUSTER, Journal of Medical Genetics, 35(1), 1998, pp. 31-36
NONHEMATOLOGICAL TRAITS ASSOCIATED WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-1 - A NEW ENTITY EMERGING
Authors: SABRY MA ZAKI M ALAWADI SA ALSALEH Q MATTAR MS
Citation: Ma. Sabry et al., NONHEMATOLOGICAL TRAITS ASSOCIATED WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-1 - A NEW ENTITY EMERGING, Clinical dysmorphology, 6(3), 1997, pp. 205-212
GENOTYPIC PHENOTYPIC HETEROGENEITY OF SELECTIVE VITAMIN-B12 MALABSORPTION (GRASBECK-IMERSLUND SYNDROME) IN 2 BEDOUIN FAMILIES/
Authors: ISMAIL EAR ALSALEH Q SABRY MA ALGHANIM M ZAKI M
Citation: Ear. Ismail et al., GENOTYPIC PHENOTYPIC HETEROGENEITY OF SELECTIVE VITAMIN-B12 MALABSORPTION (GRASBECK-IMERSLUND SYNDROME) IN 2 BEDOUIN FAMILIES/, Acta paediatrica, 86(4), 1997, pp. 424-425
ANOTHER ARAB PATIENT WITH OVERLAP OF VARADI-PAPP OPITZ TRIGONOCEPHALYSYNDROMES/
Authors: SABRY MA ALSALEH Q FARAH S OBENBERGEROVA D SIMEONOV S ALAWADI SA FARAG TI
Citation: Ma. Sabry et al., ANOTHER ARAB PATIENT WITH OVERLAP OF VARADI-PAPP OPITZ TRIGONOCEPHALYSYNDROMES/, American journal of medical genetics, 68(1), 1997, pp. 54-57
FEBRILE URINARY-TRACT INFECTION IN CHILDREN - ROLE OF TC-99M-DIMERCAPTOSUCCINIC ACID (DMSA) SCAN AND OTHER IMAGING TECHNIQUES
Authors: ZAKI M ALMUTARI G ALSALEH Q RAMADAN DG
Citation: M. Zaki et al., FEBRILE URINARY-TRACT INFECTION IN CHILDREN - ROLE OF TC-99M-DIMERCAPTOSUCCINIC ACID (DMSA) SCAN AND OTHER IMAGING TECHNIQUES, Annals of saudi medicine, 16(4), 1996, pp. 410-413
FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME WITH BIFID HALLUX, ABSENT TIBIA, AND MACROPHALLUS - A REPORT OF A BEDOUIN BABY
Authors: SABRY MA OBENBERGEROVA D ALSAWAN R ALSALEH Q FARAH S ALAWADI SA FARAG TI
Citation: Ma. Sabry et al., FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME WITH BIFID HALLUX, ABSENT TIBIA, AND MACROPHALLUS - A REPORT OF A BEDOUIN BABY, Journal of Medical Genetics, 33(2), 1996, pp. 165-167
EFFECTIVENESS OF CHLOROQUINE THERAPY IN IDIOPATHIC PULMONARY HEMOSIDEROSIS
Authors: ZAKI M ALSALEH Q ALMUTARI G
Citation: M. Zaki et al., EFFECTIVENESS OF CHLOROQUINE THERAPY IN IDIOPATHIC PULMONARY HEMOSIDEROSIS, Pediatric pulmonology, 20(2), 1995, pp. 125-126
RIGHT UPPER-LIMB BUD TRIPLICATION AND POLYTHELIA, LEFT-SIDED HEMIHYPERTROPHY AND CONGENITAL HIP DISLOCATION, FACIAL DYSMORPHISM, CONGENITALHEART-DISEASE, AND SCOLIOSIS - DISORGANIZATION-LIKE SPECTRUM OR PATTERNING GENE DEFECT
Authors: SABRY MA ALSALEH Q ALSAWAN R ALAWADI SA FARAG TI
Citation: Ma. Sabry et al., RIGHT UPPER-LIMB BUD TRIPLICATION AND POLYTHELIA, LEFT-SIDED HEMIHYPERTROPHY AND CONGENITAL HIP DISLOCATION, FACIAL DYSMORPHISM, CONGENITALHEART-DISEASE, AND SCOLIOSIS - DISORGANIZATION-LIKE SPECTRUM OR PATTERNING GENE DEFECT, Journal of Medical Genetics, 32(7), 1995, pp. 555-556
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