Citation: Avd. Kooi et al., LIMB-GIRDLE MUSCULAR-DYSTROPHY - A PATHOLOGICAL AND IMMUNOHISTOCHEMICAL REEVALUATION, Muscle & nerve, 21(5), 1998, pp. 584-590
Citation: B. Ivanyi et al., COMPUTED TOMOGRAPHIC STUDY OF THE SKELETAL MUSCULATURE OF THE LOWER-BODY IN 45 POSTPOLIO PATIENTS, Muscle & nerve, 21(4), 1998, pp. 540-542
Citation: Wgh. Oerlemans et M. Devisser, DROPPED HEAD SYNDROME AND BENT SPINE SYNDROME - 2 SEPARATE CLINICAL ENTITIES OR DIFFERENT MANIFESTATIONS OF AXIAL MYOPATHY, Journal of Neurology, Neurosurgery and Psychiatry, 65(2), 1998, pp. 258-259
Authors:
ANDRIES F
WEVERS CWJ
WINTZEN AR
BUSCH HFM
HOWELER CJ
DEJAGER AEJ
PADBERG GW
DEVISSER M
WOKKE JHJ
Citation: F. Andries et al., VOCATIONAL PERSPECTIVES AND NEUROMUSCULAR DISORDERS, International journal of rehabilitation research, 20(3), 1997, pp. 255-273
Authors:
JANSSEN EAM
KEMP S
HENSELS GW
SIE OG
DEDIESMULDERS CEM
HOOGENDIJK JE
DEVISSER M
BOLHUIS PA
Citation: Eam. Janssen et al., CONNEXIN32 GENE-MUTATIONS IN X-LINKED DOMINANT CHARCOT-MARIE-TOOTH DISEASE (CMTX1), Human genetics, 99(4), 1997, pp. 501-505
Authors:
HOOGERWAARD EM
DEVOOGT WG
WILDE AAM
VANDERWOUW PA
BAKKER E
VANOMMEN GJB
DEVISSER M
Citation: Em. Hoogerwaard et al., EVOLUTION OF CARDIAC ABNORMALITIES IN BECKER MUSCULAR-DYSTROPHY OVER A 13-YEAR PERIOD, Journal of neurology, 244(10), 1997, pp. 657-663
Authors:
VANSCHAIK IN
JOBSIS GJ
VERMEULEN M
KEIZERS H
BOLHUIS PA
DEVISSER M
Citation: In. Vanschaik et al., MACHADO-JOSEPH-DISEASE PRESENTING AS SEVERE ASYMMETRIC PROXIMAL NEUROPATHY, Journal of Neurology, Neurosurgery and Psychiatry, 63(4), 1997, pp. 534-536
Authors:
NORTH KN
LAING NG
WALLGRENPETTERSSON C
AKKARI A
BAROHN R
BARTH P
BEGGS A
DELACHAPELLE A
DEVISSER M
DUBOWITZ V
FISZMAN M
GOEBEL H
IANNACCONE S
JASANI B
LABEIT S
LAMMENS M
NAVARRO C
NEWMAN G
PELIN K
ROMERO N
SEWRY C
SLOANE A
Citation: Kn. North et al., NEMALINE MYOPATHY - CURRENT CONCEPTS, Journal of Medical Genetics, 34(9), 1997, pp. 705-713
Authors:
VANDERKOOI AJ
VANMEEGEN M
LEDDERHOF TM
MCNALLY EM
DEVISSER M
BOLHUIS PA
Citation: Aj. Vanderkooi et al., GENETIC LOCALIZATION OF A NEWLY RECOGNIZED AUTOSOMAL-DOMINANT LIMB-GIRDLE MUSCULAR-DYSTROPHY WITH CARDIAC INVOLVEMENT (LGMD1B) TO CHROMOSOME 1Q11-21, American journal of human genetics, 60(4), 1997, pp. 891-895
Authors:
JOBSIS GJ
KEIZERS H
VREIJLING JP
DEVISSER M
SPEER MC
WOLTERMAN RA
BAAS F
BOLHUIS PA
Citation: Gj. Jobsis et al., TYPE-VI COLLAGEN MUTATIONS IN BETHLEM MYOPATHY, AN AUTOSOMAL-DOMINANTMYOPATHY WITH CONTRACTURES, Nature genetics, 14(1), 1996, pp. 113-115
Authors:
COBBEN JM
SCHEFFER H
DEVISSER M
VANDERSTEEGE G
VERHEY JBBM
OSINGA J
BURTON M
MENSINK RGJ
GROOTSCHOLTEN PM
TENKATE LP
BUYS CHCM
Citation: Jm. Cobben et al., PRENATAL PREDICTION OF SPINAL MUSCULAR-ATROPHY - EXPERIENCE WITH LINKAGE STUDIES AND CONSEQUENCES OF PRESENT SMN DELETION ANALYSIS, European journal of human genetics, 4(4), 1996, pp. 231-236
Authors:
MEIJERINK PHS
HOOGENDIJK JE
GABREELSFESTEN AAWM
ZORN I
VELDMAN H
BAAS F
DEVISSER M
BOLHUIS PA
Citation: Phs. Meijerink et al., CLINICALLY DISTINCT CODON-69 MUTATIONS IN MAJOR MYELIN PROTEIN ZERO IN DEMYELINATING NEUROPATHIES, Annals of neurology, 40(4), 1996, pp. 672-675
Authors:
VANDERKOOI AJ
LEDDERHOF TM
DEVOOGT WG
RES JCJ
BOUWSMA G
TROOST D
BUSCH HFM
BECKER AE
DEVISSER M
Citation: Aj. Vanderkooi et al., A NEWLY RECOGNIZED AUTOSOMAL-DOMINANT LIMB-GIRDLE MUSCULAR-DYSTROPHY WITH CARDIAC INVOLVEMENT, Annals of neurology, 39(5), 1996, pp. 638-642
Authors:
WALLGRENPETTERSSON C
AVELA R
MARCHAND S
KOLEHMAINEN J
TAHVANAINEN E
HANSEN FJ
MUNTONI F
DUBOWITZ V
DEVISSER M
VANLANGEN IM
LAING NG
FAURE S
DELACHAPELLE A
Citation: C. Wallgrenpettersson et al., A GENE FOR AUTOSOMAL RECESSIVE NEMALINE MYOPATHY ASSIGNED TO CHROMOSOME 2Q BY LINKAGE ANALYSIS, Cytogenetics and cell genetics, 73(4), 1996, pp. 13-13
Authors:
GABREELSFESTEN AAWM
HOOGENDIJK JE
MEIJERINK PHS
GABREELS FJM
BOLHUIS PA
VANBEERSUM S
KULKENS T
NELIS E
JENNEKENS FGI
DEVISSER M
VANENGELEN BGM
VANBROECKHOVEN C
MARIMAN ECM
Citation: Aawm. Gabreelsfesten et al., 2 DIVERGENT TYPES OF NERVE PATHOLOGY IN PATIENTS WITH DIFFERENT P-0 MUTATIONS IN CHARCOT-MARIE-TOOTH DISEASE, Neurology, 47(3), 1996, pp. 761-765
Authors:
VANDERKOOI AJ
BARTH PG
BUSCH HFM
DEHAAN R
GINJAAR HB
VANESSEN AJ
VANHOOFF LJMA
HOWELER CJ
JENNEKENS FGI
JONGEN P
OOSTERHUIS HJGH
PADBERG GWAM
SPAANS F
WINTZEN AR
WOKKE JHJ
BAKKER E
VANOMMEN GJB
BOLHUIS PA
DEVISSER M
Citation: Aj. Vanderkooi et al., THE CLINICAL SPECTRUM OF LIMB-GIRDLE MUSCULAR-DYSTROPHY - A SURVEY INTHE NETHERLANDS, Brain, 119, 1996, pp. 1471-1480
Authors:
WALLGRENPETTERSSON C
AVELA K
MARCHAND S
KOLEHMAINEN J
TAHVANAINEN E
HANSEN FJ
MUNTONI F
DUBOWITZ V
DEVISSER M
VANLANGEN IM
LAING NG
FAURE S
DELACHAPELLE A
Citation: C. Wallgrenpettersson et al., A GENE FOR AUTOSOMAL RECESSIVE NEMALINE MYOPATHY ASSIGNED TO CHROMOSOME 2Q BY LINKAGE ANALYSIS, Neuromuscular disorders, 5(6), 1995, pp. 441-443