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Results: 1-23 |
Results: 23
ABSENT NAILS, KINESOGENIC CHOREOATHETOSIS, EPILEPSY AND DEVELOPMENTALDELAY - A NEW AUTOSOMAL-DOMINANT DISORDER
Authors: LYNCH SA GARDNERMEDWIN D BURN J BUSHBY KMD
Citation: Sa. Lynch et al., ABSENT NAILS, KINESOGENIC CHOREOATHETOSIS, EPILEPSY AND DEVELOPMENTALDELAY - A NEW AUTOSOMAL-DOMINANT DISORDER, Clinical dysmorphology, 6(2), 1997, pp. 133-138
CSF ANTIGLIADIN ANTIBODIES AND THE RAMSAY-HUNT-SYNDROME
Authors: CHINNERY PF READING PJ MILNE D GARDNERMEDWIN D TURNBULL DM
Citation: Pf. Chinnery et al., CSF ANTIGLIADIN ANTIBODIES AND THE RAMSAY-HUNT-SYNDROME, Neurology, 49(4), 1997, pp. 1131-1133
RESPIRATORY-CHAIN DYSFUNCTION IN PROGRESSIVE NEURONAL DEGENERATION OFCHILDHOOD WITH LIVER-DISEASE
Authors: MORRIS AAM SINGHKLER R PERRY RH GRIFFITHS PD BURT AD WONG CP GARDNERMEDWIN D TURNBULL DM
Citation: Aam. Morris et al., RESPIRATORY-CHAIN DYSFUNCTION IN PROGRESSIVE NEURONAL DEGENERATION OFCHILDHOOD WITH LIVER-DISEASE, Journal of child neurology, 11(5), 1996, pp. 417-419
FAILURE OF FIRST-LINE THERAPY WITH INTRAVENOUS IMMUNOGLOBULIN IN A CHILD WITH SCLEROMYOSITIS
Authors: ABINUN M ESTLIN E GARDNERMEDWIN D SPICKETT GP MCNEELA BJ CANT AJ
Citation: M. Abinun et al., FAILURE OF FIRST-LINE THERAPY WITH INTRAVENOUS IMMUNOGLOBULIN IN A CHILD WITH SCLEROMYOSITIS, British journal of rheumatology, 35(10), 1996, pp. 1029-1030
ARTHROGRYPOSIS MULTIPLEX CONGENITA AND BILATERAL PARIETAL POLYMICROGYRIA IN ASSOCIATION WITH THE IN INTRAUTERINE DEATH OF A TWIN
Authors: BAKER EM KHOUASGANI MG GARDNERMEDWIN D GHOLKAR A GRIFFITHS PD
Citation: Em. Baker et al., ARTHROGRYPOSIS MULTIPLEX CONGENITA AND BILATERAL PARIETAL POLYMICROGYRIA IN ASSOCIATION WITH THE IN INTRAUTERINE DEATH OF A TWIN, Neuropediatrics, 27(1), 1996, pp. 54-56
CODOMINANT INHERITANCE OF HYPEREKPLEXIA AND SPASTIC PARAPARESIS
Authors: BAXTER P CONNOLLY S CURTIS A SPENCER V RAVINDRANATH C BURN J GARDNERMEDWIN D
Citation: P. Baxter et al., CODOMINANT INHERITANCE OF HYPEREKPLEXIA AND SPASTIC PARAPARESIS, Developmental Medicine and Child Neurology, 38(8), 1996, pp. 739-743
PYRIDOXINE-DEPENDENT SEIZURES - DEMOGRAPHIC, CLINICAL, MRI AND PSYCHOMETRIC FEATURES, AND EFFECT OF DOSE ON INTELLIGENCE QUOTIENT
Authors: BAXTER P GRIFFITHS P KELLY T GARDNERMEDWIN D
Citation: P. Baxter et al., PYRIDOXINE-DEPENDENT SEIZURES - DEMOGRAPHIC, CLINICAL, MRI AND PSYCHOMETRIC FEATURES, AND EFFECT OF DOSE ON INTELLIGENCE QUOTIENT, Developmental Medicine and Child Neurology, 38(11), 1996, pp. 998-1006
CONGENITAL MYOTONIC-DYSTROPHY
Authors: THOMPSON A KAPLAN C GARDNERMEDWIN D
Citation: A. Thompson et al., CONGENITAL MYOTONIC-DYSTROPHY, Pediatric neurology, 13(1), 1995, pp. 85-85
DEFECTS OF THE NEUROMUSCULAR-JUNCTION ASSOCIATED WITH IMPAIRED NEUROMUSCULAR-TRANSMISSION IN LIMB-GIRDLE MYASTHENIAS IN MAN
Authors: SLATER CR FAWCETT PRW GARDNERMEDWIN D LYONS PR WALLS TJ WOOD SJ YOUNG C
Citation: Cr. Slater et al., DEFECTS OF THE NEUROMUSCULAR-JUNCTION ASSOCIATED WITH IMPAIRED NEUROMUSCULAR-TRANSMISSION IN LIMB-GIRDLE MYASTHENIAS IN MAN, Journal of physiology, 489P, 1995, pp. 150-151
NEW MEDICAL CLASSIFICATIONS AND LANGUAGES
Authors: GARDNERMEDWIN D
Citation: D. Gardnermedwin, NEW MEDICAL CLASSIFICATIONS AND LANGUAGES, Developmental Medicine and Child Neurology, 37(4), 1995, pp. 283-284
DELETION STATUS AND INTELLECTUAL IMPAIRMENT IN DUCHENNE MUSCULAR-DYSTROPHY
Authors: BUSHBY KMD APPLETON R ANDERSON LVB WELCH JL KELLY P GARDNERMEDWIN D
Citation: Kmd. Bushby et al., DELETION STATUS AND INTELLECTUAL IMPAIRMENT IN DUCHENNE MUSCULAR-DYSTROPHY, Developmental Medicine and Child Neurology, 37(3), 1995, pp. 260-269
NEW QUESTIONS ABOUT THE MUSCULAR-DYSTROPHIES
Authors: GARDNERMEDWIN D
Citation: D. Gardnermedwin, NEW QUESTIONS ABOUT THE MUSCULAR-DYSTROPHIES, Annals of the Rheumatic Diseases, 54(7), 1995, pp. 536-538
THALAMIC INFARCTION IN CHILDHOOD DUE TO EXTRACRANIAL VERTEBRAL ARTERYABNORMALITIES
Authors: RANDALL JM GRIFFITHS PD GARDNERMEDWIN D GHOLKAR A
Citation: Jm. Randall et al., THALAMIC INFARCTION IN CHILDHOOD DUE TO EXTRACRANIAL VERTEBRAL ARTERYABNORMALITIES, Neuropediatrics, 25(5), 1994, pp. 262-264
THE RADIOLOGICAL FEATURES OF HEMIMEGALENCEPHALY INCLUDING 3 CASES ASSOCIATED WITH PROTEUS SYNDROME
Authors: GRIFFITHS PD WELCH RJ GARDNERMEDWIN D GHOLKAR A MCALLISTER V
Citation: Pd. Griffiths et al., THE RADIOLOGICAL FEATURES OF HEMIMEGALENCEPHALY INCLUDING 3 CASES ASSOCIATED WITH PROTEUS SYNDROME, Neuropediatrics, 25(3), 1994, pp. 140-144
CHILDREN IN THE WIDER WORLD - COMPASSION AND THE SELFISH GENE
Authors: GARDNERMEDWIN D
Citation: D. Gardnermedwin, CHILDREN IN THE WIDER WORLD - COMPASSION AND THE SELFISH GENE, Developmental Medicine and Child Neurology, 36(4), 1994, pp. 283-284
THE CLINICAL, GENETIC AND DYSTROPHIN CHARACTERISTICS OF BECKER MUSCULAR-DYSTROPHY .1. NATURAL-HISTORY (VOL 240, PG 98, 1993)
Authors: BUSHBY KMD GARDNERMEDWIN D
Citation: Kmd. Bushby et D. Gardnermedwin, THE CLINICAL, GENETIC AND DYSTROPHIN CHARACTERISTICS OF BECKER MUSCULAR-DYSTROPHY .1. NATURAL-HISTORY (VOL 240, PG 98, 1993), Journal of neurology, 240(7), 1993, pp. 453-453
DYSTROPHIN EXPRESSION IN DUCHENNE PATIENTS WITH IN-FRAME GENE DELETIONS
Authors: NICHOLSON LVB BUSHBY KMD JOHNSON MA GARDNERMEDWIN D GINJAAR IB
Citation: Lvb. Nicholson et al., DYSTROPHIN EXPRESSION IN DUCHENNE PATIENTS WITH IN-FRAME GENE DELETIONS, Neuropediatrics, 24(2), 1993, pp. 93-97
INTEGRATED STUDY OF 100 PATIENTS WITH XP21 LINKED MUSCULAR-DYSTROPHY USING CLINICAL, GENETIC, IMMUNOCHEMICAL, AND HISTOPATHOLOGICAL DATA .1. TRENDS ACROSS THE CLINICAL GROUPS
Authors: NICHOLSON LVB JOHNSON MA BUSHBY KMD GARDNERMEDWIN D CURTIS A GINJAAR IB DENDUNNEN JT WELCH JL BUTLER TJ BAKKER E VANOMMEN GJB HARRIS JB
Citation: Lvb. Nicholson et al., INTEGRATED STUDY OF 100 PATIENTS WITH XP21 LINKED MUSCULAR-DYSTROPHY USING CLINICAL, GENETIC, IMMUNOCHEMICAL, AND HISTOPATHOLOGICAL DATA .1. TRENDS ACROSS THE CLINICAL GROUPS, Journal of Medical Genetics, 30(9), 1993, pp. 728-736
INTEGRATED STUDY OF 100 PATIENTS WITH XP21 LINKED MUSCULAR-DYSTROPHY USING CLINICAL, GENETIC, IMMUNOCHEMICAL, AND HISTOPATHOLOGICAL DATA .2. CORRELATIONS WITHIN INDIVIDUAL PATIENTS
Authors: NICHOLSON LVB JOHNSON MA BUSHBY KMD GARDNERMEDWIN D CURTIS A GINJAAR IB DENDUNNEN JT WELCH JL BUTLER TJ BAKKER E VANOMMEN GJB HARRIS JB
Citation: Lvb. Nicholson et al., INTEGRATED STUDY OF 100 PATIENTS WITH XP21 LINKED MUSCULAR-DYSTROPHY USING CLINICAL, GENETIC, IMMUNOCHEMICAL, AND HISTOPATHOLOGICAL DATA .2. CORRELATIONS WITHIN INDIVIDUAL PATIENTS, Journal of Medical Genetics, 30(9), 1993, pp. 737-744
INTEGRATED STUDY OF 100 PATIENTS WITH XP21 LINKED MUSCULAR-DYSTROPHY USING CLINICAL, GENETIC, IMMUNOCHEMICAL, AND HISTOPATHOLOGICAL DATA .3. DIFFERENTIAL-DIAGNOSIS AND PROGNOSIS
Authors: NICHOLSON LVB JOHNSON MA BUSHBY KMD GARDNERMEDWIN D CURTIS A GINJAAR IB DENDUNNEN JT WELCH JL BUTLER TJ BAKKER E VANOMMEN GJB HARRIS JB
Citation: Lvb. Nicholson et al., INTEGRATED STUDY OF 100 PATIENTS WITH XP21 LINKED MUSCULAR-DYSTROPHY USING CLINICAL, GENETIC, IMMUNOCHEMICAL, AND HISTOPATHOLOGICAL DATA .3. DIFFERENTIAL-DIAGNOSIS AND PROGNOSIS, Journal of Medical Genetics, 30(9), 1993, pp. 745-751
OROFACIODIGITAL SYNDROME TYPE-III IN 2 SIBS
Authors: SMITH RA GARDNERMEDWIN D
Citation: Ra. Smith et D. Gardnermedwin, OROFACIODIGITAL SYNDROME TYPE-III IN 2 SIBS, Journal of Medical Genetics, 30(10), 1993, pp. 870-872
CONGENITAL LIVEDO-RETICULARIS AND RECURRENT STROKE-LIKE EPISODES
Authors: BAXTER P GARDNERMEDWIN D GREEN SH MOSS C
Citation: P. Baxter et al., CONGENITAL LIVEDO-RETICULARIS AND RECURRENT STROKE-LIKE EPISODES, Developmental Medicine and Child Neurology, 35(10), 1993, pp. 917-921
FUNCTIONAL-SIGNIFICANCE OF DYSTROPHIN POSITIVE FIBERS IN DUCHENNE MUSCULAR-DYSTROPHY
Authors: NICHOLSON LVB JOHNSON MA BUSHBY KMD GARDNERMEDWIN D
Citation: Lvb. Nicholson et al., FUNCTIONAL-SIGNIFICANCE OF DYSTROPHIN POSITIVE FIBERS IN DUCHENNE MUSCULAR-DYSTROPHY, Archives of Disease in Childhood, 68(5), 1993, pp. 632-636
Risultati: 1-23 |