Authors:
AINSWORTH PJ
BOLTON CF
MURPHY BC
STUART JA
HAHN AF
Citation: Pj. Ainsworth et al., GENOTYPE PHENOTYPE CORRELATION IN AFFECTED INDIVIDUALS OF A FAMILY WITH A DELETION OF THE ENTIRE CODING SEQUENCE OF THE CONNEXIN-32 GENE/, Human genetics, 103(2), 1998, pp. 242-244
Authors:
HIRANO M
GARCIADEYEBENES J
JONES AC
NISHINO I
DIMAURO S
CARLO JR
BENDER AN
HAHN AF
SALBERG LM
WEEKS DE
NYGAARD TG
Citation: M. Hirano et al., MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY SYNDROME MAPS TO CHROMOSOME 22Q13.32-QTER, American journal of human genetics, 63(2), 1998, pp. 526-533
Citation: Pj. Ainsworth et al., GENOTYPE PHENOTYPE CORRELATION IN AFFECTED INDIVIDUALS OF A FAMILY WITH A DELETION OF THE ENTIRE CODING SEQUENCE OF THE CONNEXIN-32 GENE/, American journal of human genetics, 61(4), 1997, pp. 1901-1901
Authors:
BULMAN DE
VANOENE MD
HAHN AF
TOLLAR LL
EBERS GC
Citation: De. Bulman et al., A NOVEL SODIUM-CHANNEL MUTATION CAUSING HYPOKALEMIC PERIODIC PARALYSIS, American journal of human genetics, 61(4), 1997, pp. 1914-1914
Citation: Cc. Tan et al., NOVEL MUTATIONS IN THE CONNEXIN-32 GENE ASSOCIATED WITH X-LINKED CHARCOT-MARIE-TOOTH-DISEASE, Human mutation, 7(2), 1996, pp. 167-171
Authors:
TAN CC
AINSWORTH PJ
IONASESCU V
BOLTON CF
HAHN AF
Citation: Cc. Tan et al., X-LINKED DOMINANT CHARCOT-MARIE-TOOTH DISEASE - NOVEL CONNEXIN-32 MUTATIONS AND THEIR RELATIONSHIP TO CLINICAL AND PATHOLOGICAL DISEASE, Annals of neurology, 40(3), 1996, pp. 215-215
Citation: Af. Hahn, EXPERIMENTAL ALLERGIC NEURITIS (EAN) AS A MODEL FOR THE IMMUNE-MEDIATED DEMYELINATING NEUROPATHIES, Revue neurologique, 152(5), 1996, pp. 328-332
Authors:
ZIFKO U
CHEN R
REMTULLA H
HAHN AF
KOOPMAN W
BOLTON CF
Citation: U. Zifko et al., RESPIRATORY ELECTROPHYSIOLOGICAL STUDIES IN GUILLAIN-BARRE-SYNDROME, Journal of Neurology, Neurosurgery and Psychiatry, 60(2), 1996, pp. 191-194
Authors:
HAHN AF
BOLTON CF
VANDERVOORT M
PILAY N
CHALK C
BENSTEAD T
BRIL V
FEASBY TE
Citation: Af. Hahn et al., PLASMA-EXCHANGE THERAPY IN CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY - A DOUBLE-BLIND, SHAM-CONTROLLED CROSSOVER STUDY, Annals of neurology, 38(2), 1995, pp. 303-303
Authors:
ZIFKO U
CHEN R
REMTULLA H
HAHN AF
KOOPMAN W
BOLTON CF
Citation: U. Zifko et al., ELECTROPHYSIOLOGICAL STUDIES OF THE DIAPHRAGM IN ACUTE INFLAMMATORY DEMYELINATING POLYNEUROPATHY, Annals of neurology, 38(2), 1995, pp. 307-307
Authors:
BULMAN DE
VONBREDERLOW B
HAHN AF
KOOPMAN WJ
EBERS GC
Citation: De. Bulman et al., MAPPING THE GENE FOR ACETAZOLAMIDE-RESPONSIVE HEREDITARY PAROXYSMAL CEREBELLAR-ATAXIA TO CHROMOSOME-19P, Neurology, 45(4), 1995, pp. 421-421
Citation: Te. Feasby et al., LEWIS RAT EAN IS SUPPRESSED BY THE 21-AMINOSTEROID TIRILAZAD MESYLATE(U-74006F), Neuropathology and applied neurobiology, 20(4), 1994, pp. 384-391