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Results: 1-10 |
Results: 10
DEL(18P) SHOWN TO BE A CRYPTIC TRANSLOCATION USING A MULTIPROBE FISH ASSAY FOR SUBTELOMERIC CHROMOSOME REARRANGEMENTS
Authors: HORSLEY SW KNIGHT SJL NIXON J HUSON S FITCHETT M BOONE RA HILTONJONES D FLINT J KEARNEY L
Citation: Sw. Horsley et al., DEL(18P) SHOWN TO BE A CRYPTIC TRANSLOCATION USING A MULTIPROBE FISH ASSAY FOR SUBTELOMERIC CHROMOSOME REARRANGEMENTS, Journal of Medical Genetics, 35(9), 1998, pp. 722-726
MYOTONIC-DYSTROPHY - FORGOTTEN ASPECTS OF AN OFTEN NEGLECTED CONDITION
Authors: HILTONJONES D
Citation: D. Hiltonjones, MYOTONIC-DYSTROPHY - FORGOTTEN ASPECTS OF AN OFTEN NEGLECTED CONDITION, Current opinion in neurology, 10(5), 1997, pp. 399-401
DYSTROBREVIN DEFICIENCY AT THE SARCOLEMMA OF PATIENTS WITH MUSCULAR-DYSTROPHY
Authors: METZINGER L BLAKE DJ SQUIER MV ANDERSON LVB DECONINCK AE NAWROTZKI R HILTONJONES D DAVIES KE
Citation: L. Metzinger et al., DYSTROBREVIN DEFICIENCY AT THE SARCOLEMMA OF PATIENTS WITH MUSCULAR-DYSTROPHY, Human molecular genetics, 6(7), 1997, pp. 1185-1191
MUSCLE X-INACTIVATION PATTERNS AND DYSTROPHIN EXPRESSION IN DUCHENNE MUSCULAR-DYSTROPHY CARRIERS
Authors: MATTHEWS PM BENJAMIN D VANBAKEL I SQUIER MV NICHOLSON LVB SEWRY C BARNES PRJ HOPKIN J BROWN R HILTONJONES D BOYD Y KARPATI G BROWN GK CRAIG IW
Citation: Pm. Matthews et al., MUSCLE X-INACTIVATION PATTERNS AND DYSTROPHIN EXPRESSION IN DUCHENNE MUSCULAR-DYSTROPHY CARRIERS, Neuromuscular disorders, 5(3), 1995, pp. 209-220
RECURRENT CONGENITAL ARTHROGRYPOSIS LEADING TO A DIAGNOSIS OF MYASTHENIA-GRAVIS IN AN INITIALLY ASYMPTOMATIC MOTHER
Authors: BARNES PRJ KANABAR DJ BRUETON L NEWSOMDAVIS J HUSON SM MANN NP HILTONJONES D
Citation: Prj. Barnes et al., RECURRENT CONGENITAL ARTHROGRYPOSIS LEADING TO A DIAGNOSIS OF MYASTHENIA-GRAVIS IN AN INITIALLY ASYMPTOMATIC MOTHER, Neuromuscular disorders, 5(1), 1995, pp. 59-65
SPONTANEOUS INTRACRANIAL HYPOTENSION
Authors: RENOWDEN SA GREGORY R HYMAN N HILTONJONES D
Citation: Sa. Renowden et al., SPONTANEOUS INTRACRANIAL HYPOTENSION, Journal of Neurology, Neurosurgery and Psychiatry, 59(5), 1995, pp. 511-515
DEATH AFTER ECSTASY INGESTION - NEUROPATHOLOGICAL FINDINGS
Authors: SQUIER MV JALLOH S HILTONJONES D SERIES H
Citation: Mv. Squier et al., DEATH AFTER ECSTASY INGESTION - NEUROPATHOLOGICAL FINDINGS, Journal of Neurology, Neurosurgery and Psychiatry, 58(6), 1995, pp. 756-756
INCORRECT DIAGNOSIS OF MYOTONIC-DYSTROPHY AND ITS POTENTIAL CONSEQUENCES REVEALED BY SUBSEQUENT DIRECT GENETIC-ANALYSIS
Authors: BARNES PRJ HILTONJONES D NORBURY G ROBERTS A HUSON SM
Citation: Prj. Barnes et al., INCORRECT DIAGNOSIS OF MYOTONIC-DYSTROPHY AND ITS POTENTIAL CONSEQUENCES REVEALED BY SUBSEQUENT DIRECT GENETIC-ANALYSIS, Journal of Neurology, Neurosurgery and Psychiatry, 57(5), 1994, pp. 662-662
COMPARISON OF THE RELATIVE LEVELS OF THE 3243 (A-]G) MTDNA MUTATION IN HETEROPLASMIC ADULT AND FETAL TISSUES
Authors: MATTHEWS PM HOPKIN J BROWN RM STEPHENSON JBP HILTONJONES D BROWN GK
Citation: Pm. Matthews et al., COMPARISON OF THE RELATIVE LEVELS OF THE 3243 (A-]G) MTDNA MUTATION IN HETEROPLASMIC ADULT AND FETAL TISSUES, Journal of Medical Genetics, 31(1), 1994, pp. 41-44
MOLECULAR-GENETICS OF MYOTONIC-DYSTROPHY
Authors: BARNES PRJ HILTONJONES D
Citation: Prj. Barnes et D. Hiltonjones, MOLECULAR-GENETICS OF MYOTONIC-DYSTROPHY, British Journal of Hospital Medicine, 50(7), 1993, pp. 425-425
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