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Results: 1-17 |
Results: 17
Neuronal migration defects in the Dreher (Lmx1a) mutant mouse: Role of disorders of the glial limiting membrane
Authors: Costa, C Harding, B Copp, AJ
Citation: C. Costa et al., Neuronal migration defects in the Dreher (Lmx1a) mutant mouse: Role of disorders of the glial limiting membrane, CEREB CORT, 11(6), 2001, pp. 498-505
Gain of 1q and loss of 22 are the most common changes detected by comparative genomic hybridisation in paediatric ependymoma
Authors: Ward, S Harding, B Wilkins, P Harkness, W Hayward, R Darling, JL Thomas, DGT Warr, T
Citation: S. Ward et al., Gain of 1q and loss of 22 are the most common changes detected by comparative genomic hybridisation in paediatric ependymoma, GENE CHROM, 32(1), 2001, pp. 59-66
Identification of extensive genomic loss and gain by comparative genomic hybridisation in malignant astrocytoma in children and young adults
Authors: Warr, T Ward, S Burrows, L Harding, B Wilkins, P Harkness, W Hayward, R Darling, J Thomas, D
Citation: T. Warr et al., Identification of extensive genomic loss and gain by comparative genomic hybridisation in malignant astrocytoma in children and young adults, GENE CHROM, 31(1), 2001, pp. 15-22
Bilateral hippocampal granule cell dispersion: autopsy study of 3 infants
Authors: Harding, B Thom, M
Citation: B. Harding et M. Thom, Bilateral hippocampal granule cell dispersion: autopsy study of 3 infants, NEUROP AP N, 27(3), 2001, pp. 245-251
Absence of mutations in the growth hormone (GH)-releasing hormone receptorgene in GH-secreting pituitary adenomas
Authors: Salvatori, R Thakker, RV Lopes, MB Fan, XG Eswara, JR Ellison, D Lees, P Harding, B Yang, IM Levine, MA
Citation: R. Salvatori et al., Absence of mutations in the growth hormone (GH)-releasing hormone receptorgene in GH-secreting pituitary adenomas, CLIN ENDOCR, 54(3), 2001, pp. 301-307
X-linked hypophosphatemia attributable to pseudoexons of the PHEX gene
Authors: Christie, PT Harding, B Nesbit, MA Whyte, MP Thakker, RV
Citation: Pt. Christie et al., X-linked hypophosphatemia attributable to pseudoexons of the PHEX gene, J CLIN END, 86(8), 2001, pp. 3840-3844
Chromosomal aberrations in sporadic pituitary tumors
Authors: Trautmann, K Thakker, RV Ellison, DW Ibrahim, A Lees, PD Harding, B Fischer, C Popp, S Bartram, CR Jauch, A
Citation: K. Trautmann et al., Chromosomal aberrations in sporadic pituitary tumors, INT J CANC, 91(6), 2001, pp. 809-814
Chemosensitivity in childhood brain tumours in vitro: evidence of differential sensitivity to lomustine (CCNU) and vincristine
Authors: Lewandowicz, GM Harding, B Harkness, W Hayward, R Thomas, DGT Darling, JL
Citation: Gm. Lewandowicz et al., Chemosensitivity in childhood brain tumours in vitro: evidence of differential sensitivity to lomustine (CCNU) and vincristine, EUR J CANC, 36(15), 2000, pp. 1955-1964
GATA3 haplo-insufficiency causes human HDR syndrome
Authors: Van Esch, H Groenen, P Nesbit, MA Schuffenhauer, S Lichtner, P Vanderlinden, G Harding, B Beetz, R Bilous, RW Holdaway, I Shaw, NJ Fryns, JP Van de Ven, WV Thakker, RV Devriendt, K
Citation: H. Van Esch et al., GATA3 haplo-insufficiency causes human HDR syndrome, NATURE, 406(6794), 2000, pp. 419-422
A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred
Authors: Mumm, S Christie, PT Finnegan, P Jones, J Dixon, PH Pannett, AAJ Harding, B Gottesman, GS Thakker, RV Whyte, MP
Citation: S. Mumm et al., A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred, J CLIN END, 85(9), 2000, pp. 3343-3347
Acute disseminated encephalomyelitis, multiphasic disseminated encephalomyelitis and multiple sclerosis in children
Authors: Dale, RC de Sousa, C Chong, WK Cox, TCS Harding, B Neville, BGR
Citation: Rc. Dale et al., Acute disseminated encephalomyelitis, multiphasic disseminated encephalomyelitis and multiple sclerosis in children, BRAIN, 123, 2000, pp. 2407-2422
Neuropathology
Authors: Harding, B
Citation: B. Harding, Neuropathology, CONGENITAL HEMIPLEGIA, 2000, pp. 18-25
Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31 (vol 14, pg 230, 1999)
Authors: Williamson, C Cavaco, BM Jauch, A Dixon, PH Forbes, S Harding, B Holtgreve-Grez, H Schoell, B Pereira, MC Font, AP Loureiro, MM Sobrinho, LG Santos, MA Thakker, RV
Citation: C. Williamson et al., Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31 (vol 14, pg 230, 1999), J BONE MIN, 14(8), 1999, pp. 1472-1472
Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31
Authors: Williamson, C Cavaco, BM Jausch, A Dixon, P Forbes, S Harding, B Holtgreve-Grez, H Schoell, B Pereira, MC Font, AP Loureiro, MM Sobrinho, LG Santos, MA Thakker, RV
Citation: C. Williamson et al., Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31, J BONE MIN, 14(2), 1999, pp. 230-239
Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1
Authors: Bassett, JHD Rashbass, P Harding, B Forbes, SA Pannett, AAJ Thakker, RV
Citation: Jhd. Bassett et al., Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1, J BONE MIN, 14(1), 1999, pp. 3-10
Neuropathology: A reference text of CNS pathology (vol 123, pg 445, 1999)
Authors: Ellison, D Love, S Chimelli, L Harding, B Lowe, J Roberts, GW Vinters, HV
Citation: D. Ellison et al., Neuropathology: A reference text of CNS pathology (vol 123, pg 445, 1999), ARCH PATH L, 123(9), 1999, pp. 859-859
Ki-67 immunolabelling index is a prognostic indicator in childhood posterior fossa ependymomas
Authors: Bennetto, L Foreman, N Harding, B Hayward, R Ironside, J Love, S Ellison, D
Citation: L. Bennetto et al., Ki-67 immunolabelling index is a prognostic indicator in childhood posterior fossa ependymomas, NEUROP AP N, 24(6), 1998, pp. 434-440
Risultati: 1-17 |