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Results: 1-21 |
Results: 21
THE AUTOSOMAL RECESSIVE CONGENITAL INTRAUTERINE INFECTION-LIKE SYNDROME OF MICROCEPHALY, INTRACRANIAL CALCIFICATION, AND CNS DISEASE - REPORT OF ANOTHER BEDOUIN FAMILY
Authors: ALDABBOUS R SABRY MA FARAH S ALAWADI SA SIMEONOV S FARAG TI
Citation: R. Aldabbous et al., THE AUTOSOMAL RECESSIVE CONGENITAL INTRAUTERINE INFECTION-LIKE SYNDROME OF MICROCEPHALY, INTRACRANIAL CALCIFICATION, AND CNS DISEASE - REPORT OF ANOTHER BEDOUIN FAMILY, Clinical dysmorphology, 7(2), 1998, pp. 127-130
CUTIS-VERTICIS-GYRATA-MENTAL-DEFICIENCY-SYNDROME - REPORT OF A CASE WITH UNUSUAL NEURORADIOLOGICAL FINDINGS
Authors: FARAH S FARAG T SABRY MA SIMEONOV ST ALKHATTAM S ABULHASSAN SJ QUASRAWI B ALBUSAIRI W ALAWADI SA
Citation: S. Farah et al., CUTIS-VERTICIS-GYRATA-MENTAL-DEFICIENCY-SYNDROME - REPORT OF A CASE WITH UNUSUAL NEURORADIOLOGICAL FINDINGS, Clinical dysmorphology, 7(2), 1998, pp. 131-134
BEHCETS-SYNDROME - A REPORT OF 41 PATIENTS WITH EMPHASIS ON NEUROLOGICAL MANIFESTATIONS
Authors: FARAH S ALSHUBAILI A MONTASER A HUSSEIN JM MALAVIYA AN MUKHTAR M ALSHAYEB A KHURAIBET AJ KHAN R TRONTELJ JV
Citation: S. Farah et al., BEHCETS-SYNDROME - A REPORT OF 41 PATIENTS WITH EMPHASIS ON NEUROLOGICAL MANIFESTATIONS, Journal of Neurology, Neurosurgery and Psychiatry, 64(3), 1998, pp. 382-384
ROBINOW-SYNDROME - REPLY
Authors: SABRY MA ISMAIL EAR ALTORKI NA FARAH S
Citation: Ma. Sabry et al., ROBINOW-SYNDROME - REPLY, Journal of Medical Genetics, 35(4), 1998, pp. 350-350
TRIOPHTHALMIA AND FACIAL CLEFTING - A CASE-REPORT
Authors: TAYEL SM SABRY MA ABDELKADER N FARAH S ALAWADI SA FARAG TI
Citation: Sm. Tayel et al., TRIOPHTHALMIA AND FACIAL CLEFTING - A CASE-REPORT, Journal of Medical Genetics, 35(10), 1998, pp. 875-877
A RHO-ASSOCIATED PROTEIN-KINASE, ROK-ALPHA, BINDS INSULIN-RECEPTOR SUBSTRATE-1 AND MODULATES INSULIN SIGNALING
Authors: FARAH S AGAZIE Y OHAN N NGSEE JK LIU XJ
Citation: S. Farah et al., A RHO-ASSOCIATED PROTEIN-KINASE, ROK-ALPHA, BINDS INSULIN-RECEPTOR SUBSTRATE-1 AND MODULATES INSULIN SIGNALING, The Journal of biological chemistry, 273(8), 1998, pp. 4740-4746
MOLECULAR-CLONING AND CHARACTERIZATION OF XENOPUS INSULIN-LIKE GROWTH-FACTOR-I RECEPTOR - ITS ROLE IN MEDIATING INSULIN-INDUCED XENOPUS OOCYTE MATURATION AND EXPRESSION DURING EMBRYOGENESIS
Authors: ZHU L OHAN N AGAZIE Y CUMMINGS C FARAH S LIU XJ
Citation: L. Zhu et al., MOLECULAR-CLONING AND CHARACTERIZATION OF XENOPUS INSULIN-LIKE GROWTH-FACTOR-I RECEPTOR - ITS ROLE IN MEDIATING INSULIN-INDUCED XENOPUS OOCYTE MATURATION AND EXPRESSION DURING EMBRYOGENESIS, Endocrinology, 139(3), 1998, pp. 949-954
HEREDITARY SPASTIC PARAPARESIS WITH DISTAL MUSCLE WASTING, MICROCEPHALY, MENTAL-RETARDATION, ARACHNODACTYLY AND TREMORS - NEW ENTITY
Authors: FARAH S SABRY MA ALSHUBAILI AFK ANIM JT HUSSAIN JM MONTASER MA SHARFUDDIN KM
Citation: S. Farah et al., HEREDITARY SPASTIC PARAPARESIS WITH DISTAL MUSCLE WASTING, MICROCEPHALY, MENTAL-RETARDATION, ARACHNODACTYLY AND TREMORS - NEW ENTITY, Clinical neurology and neurosurgery, 99(1), 1997, pp. 66-70
BUDD-CHIARI-SYNDROME - A REVIEW OF 10 CASES
Authors: FARAH S UTHMAN S ABYAD A
Citation: S. Farah et al., BUDD-CHIARI-SYNDROME - A REVIEW OF 10 CASES, Journal of international medical research, 25(3), 1997, pp. 171-174
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
UNUSUAL TRAITS ASSOCIATED WITH ROBINOW-SYNDROME
Authors: SABRY MA ISMAIL EAR ALNAGGAR RL ALTORKI NA FARAH S ALAWADI SA OBENBERGEROVA D BASTAKI L
Citation: Ma. Sabry et al., UNUSUAL TRAITS ASSOCIATED WITH ROBINOW-SYNDROME, Journal of Medical Genetics, 34(9), 1997, pp. 736-740
LISSENCEPHALY ASSOCIATED WITH CEREBELLAR HYPOPLASIA AND MYOCLONIC EPILEPSY IN A BEDOUIN KINDRED - A NEW SYNDROME
Authors: FARAH S SABRY MA KHURAIBET A KHAFFAGI S RUDWAN M HASSAN M HASEEB N ABULHASSAN S ABDELRASOOL MA ELGAMAL S QASRAWI B ALBUSAIRI W FARAG TI
Citation: S. Farah et al., LISSENCEPHALY ASSOCIATED WITH CEREBELLAR HYPOPLASIA AND MYOCLONIC EPILEPSY IN A BEDOUIN KINDRED - A NEW SYNDROME, Clinical genetics, 51(5), 1997, pp. 326-330
IDENTIFICATION OF CHROMOSOME 15Q11-12 HAPLO-INSUFFIENCY IN THE AUTISTIC DISORDER
Authors: SABRY MA ALSHUBAILI A MAGHRABI MA FARAH S ABULHASSAN SJ RASOOL MAA ALAWADI SA
Citation: Ma. Sabry et al., IDENTIFICATION OF CHROMOSOME 15Q11-12 HAPLO-INSUFFIENCY IN THE AUTISTIC DISORDER, American journal of human genetics, 61(4), 1997, pp. 2193-2193
MARINESCO-SJOGREN-SYNDROME IN A BEDOUIN FAMILY
Authors: FARAH S SABRY MA KHURAIBET AJ ANIM JT QUASRAWI B ALKHATAM S ALBUSAIRI W HUSSEIN JM KHAN RA ALAWADI SA
Citation: S. Farah et al., MARINESCO-SJOGREN-SYNDROME IN A BEDOUIN FAMILY, Acta neurologica Scandinavica, 96(6), 1997, pp. 387-391
HUMAN Y-CHROMOSOME AZOOSPERMIA FACTORS (AZF) MAPPED TO DIFFERENT SUBREGIONS IN YQ11
Authors: VOGT PH EDELMANN A KIRSCH S HENEGARIU O HIRSCHMANN P KIESEWETTER F KOHN FM SCHILL WB FARAH S RAMOS C HARTMANN M HARTSCHUH W MESCHEDE D BEHRE HM CASTEL A NIESCHLAG E WEIDNER W GRONE HJ JUNG A ENGEL W HAIDL G
Citation: Ph. Vogt et al., HUMAN Y-CHROMOSOME AZOOSPERMIA FACTORS (AZF) MAPPED TO DIFFERENT SUBREGIONS IN YQ11, Human molecular genetics, 5(7), 1996, pp. 933-943
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
MOLECULAR CHARACTERIZATION OF HUMAN T-LYMPHOTROPIC VIRUS, TYPE-1 (HTLV-1) FOUND IN KUWAIT - CLOSE SIMILARITY WITH HTLV-1 ISOLATES ORIGINATING FROM MASHHAD, IRAN
Authors: VOEVODIN A ALMUFTI S FARAH S KHAN R MIURA T
Citation: A. Voevodin et al., MOLECULAR CHARACTERIZATION OF HUMAN T-LYMPHOTROPIC VIRUS, TYPE-1 (HTLV-1) FOUND IN KUWAIT - CLOSE SIMILARITY WITH HTLV-1 ISOLATES ORIGINATING FROM MASHHAD, IRAN, AIDS research and human retroviruses, 11(10), 1995, pp. 1255-1259
EXTERNAL FIXATION OF INTERTROCHANTERIC FR ACTURES OF THE FEMUR
Authors: BARROS JW FERREIRA CD FREITAS AA FARAH S
Citation: Jw. Barros et al., EXTERNAL FIXATION OF INTERTROCHANTERIC FR ACTURES OF THE FEMUR, International orthopaedics, 19(4), 1995, pp. 217-219
MILLER-FISHER-SYNDROME - UNIQUE INVOLVEMENT OF OPHTHALMIC DIVISION OFTRIGEMINAL NERVE
Authors: FARAH S KHURAIBET AJ MONTASER MA HUSSAIN HM
Citation: S. Farah et al., MILLER-FISHER-SYNDROME - UNIQUE INVOLVEMENT OF OPHTHALMIC DIVISION OFTRIGEMINAL NERVE, Clinical neurology and neurosurgery, 97(4), 1995, pp. 328-331
A POSSIBLE NEW VARIANT OF NONSYNDROMIC LISSENCEPHALY, ASSOCIATED WITHMYOCLONIC EPILEPSY
Authors: FARAH S RUDWAN M KHAFAGI S KHURAIBET A QASRAWI B ALBUSAIRI W HASSAN M HASSEEB N ELGAMAL SA SABRY MA FARAG TI
Citation: S. Farah et al., A POSSIBLE NEW VARIANT OF NONSYNDROMIC LISSENCEPHALY, ASSOCIATED WITHMYOCLONIC EPILEPSY, American journal of human genetics, 57(4), 1995, pp. 1773-1773
IMMUNOHISTOCHEMISTRY OF INFILTRATING LYMPHOCYTES IN UVEAL MALIGNANT-MELANOMA
Authors: FARAH S WHELCHEL JC MCLEAN IW BURNIER MM
Citation: S. Farah et al., IMMUNOHISTOCHEMISTRY OF INFILTRATING LYMPHOCYTES IN UVEAL MALIGNANT-MELANOMA, Investigative ophthalmology & visual science, 33(4), 1992, pp. 1242-1242
Risultati: 1-21 |