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Results: 1-8 |
Results: 8
Congenital insensitivity to pain with anhidrosis (CIPA): Novel mutations of the TRK4 (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency
Authors: Indo, Y Mardy, S Miura, Y Moosa, A Ismail, EAR Toscano, E Andria, G Pavone, V Brown, DL Brooks, A Endo, F Matsuda, I
Citation: Y. Indo et al., Congenital insensitivity to pain with anhidrosis (CIPA): Novel mutations of the TRK4 (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency, HUM MUTAT, 18(4), 2001, pp. 308-318
A case of non-0 : 1 Vibrio cholerae septicemia with meningitis, cerebral abscess and unilateral hydrocephalus in a preterm baby
Authors: Ismail, EAR Shafik, MH Al-Mutairi, G
Citation: Ear. Ismail et al., A case of non-0 : 1 Vibrio cholerae septicemia with meningitis, cerebral abscess and unilateral hydrocephalus in a preterm baby, EUR J CL M, 20(8), 2001, pp. 598-600
Incomplete form of chronic infantile neurological cutaneous and articular syndrome
Authors: Ismail, EAR
Citation: Ear. Ismail, Incomplete form of chronic infantile neurological cutaneous and articular syndrome, PEDIATR INT, 42(5), 2000, pp. 592-592
A fatal small dose of phosphate enema in a young child with no renal or gastrointestinal abnormality
Authors: Ismail, EAR Al-Mutairi, G Al-Anzy, H
Citation: Ear. Ismail et al., A fatal small dose of phosphate enema in a young child with no renal or gastrointestinal abnormality, J PED GASTR, 30(2), 2000, pp. 220-221
Fucosidosis: immunological studies and chronological neuroradiological changes
Authors: Ismail, EAR Rudwan, M Shafik, MH
Citation: Ear. Ismail et al., Fucosidosis: immunological studies and chronological neuroradiological changes, ACT PAEDIAT, 88(2), 1999, pp. 224-227
Persistent hyperinsulinaemic hypoglycaemia of infancy (nesidioblastosis): a report from Kuwait
Authors: Ramadan, DG Badawi, MH Zaki, M El Mazidi, Z Ismail, EAR El Anzi, H
Citation: Dg. Ramadan et al., Persistent hyperinsulinaemic hypoglycaemia of infancy (nesidioblastosis): a report from Kuwait, ANN TROP PA, 19(1), 1999, pp. 55-59
Congenital insensitivity to pain with anhidrosis: Novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor
Authors: Mardy, S Miura, Y Endo, F Matsuda, I Sztriha, L Frossard, P Moosa, A Ismail, EAR Macaya, A Andria, G Toscano, E Gibson, W Graham, GE Indo, Y
Citation: S. Mardy et al., Congenital insensitivity to pain with anhidrosis: Novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor, AM J HU GEN, 64(6), 1999, pp. 1570-1579
Congenital insensitivity to pain with anhidrosis: Lack of eccrine sweat gland innervation confirmed (vol 13, pg 243, 1998)
Authors: Ismail, EAR Al-Shammari, N Amin, JT Moosa, A
Citation: Ear. Ismail et al., Congenital insensitivity to pain with anhidrosis: Lack of eccrine sweat gland innervation confirmed (vol 13, pg 243, 1998), J CHILD NEU, 13(12), 1998, pp. 632-632
Risultati: 1-8 |