Authors:
DEJONGHE P
TIMMERMAN V
FITZPATRICK D
SPOELDERS P
MARTIN JJ
VANBROECKHOVEN C
Citation: P. Dejonghe et al., MUTILATING NEUROPATHIC ULCERATIONS IN A CHROMOSOME 3Q13-Q22 LINKED CHARCOT-MARIE-TOOTH DISEASE TYPE 2B FAMILY, Journal of Neurology, Neurosurgery and Psychiatry, 62(6), 1997, pp. 570-573
Authors:
TIMMERMAN V
RAUTENSTRAUSS B
REITER LT
KOEUTH T
LOFGREN A
LIEHR T
NELIS E
BATHKE KD
DEJONGHE P
GREHL H
MARTIN JJ
LUPSKI JR
VANBROECKHOVEN C
Citation: V. Timmerman et al., DETECTION OF THE CMT1A HNPP RECOMBINATION HOTSPOT IN UNRELATED PATIENTS OF EUROPEAN DESCENT/, Journal of Medical Genetics, 34(1), 1997, pp. 43-49
Authors:
OKOCHI M
ISHII K
USAMI M
SAHARA N
KAMETANI F
TANAKA K
FRASER PE
IKEDA M
SAUNDERS AM
HENDRIKS L
SHOJI SI
NEE LE
MARTIN JJ
VANBROECKHOVEN C
STGEORGEHYSLOP PH
ROSES AD
MORI H
Citation: M. Okochi et al., PROTEOLYTIC PROCESSING OF PRESENILIN-1 (PS-1) IS NOT ASSOCIATED WITH ALZHEIMERS-DISEASE WITH OR WITHOUT PS-1 MUTATIONS, FEBS letters, 418(1-2), 1997, pp. 162-166
Authors:
BEUTEN J
DEJONGHE P
CEUTERICK C
MARTIN JJ
VANBROECKHOVEN C
TIMMERMAN V
Citation: J. Beuten et al., CONSTRUCTION OF A YAC CONTIG OF THE 12Q24 REGION FOR THE FINE MAPPINGOF A LOCUS FOR DISTAL HEREDITARY MOTOR NEUROPATHY TYPE-II, American journal of human genetics, 61(4), 1997, pp. 1343-1343
Authors:
SPOELDERS P
LOFGREN A
DEJONGHE P
NELIS E
MARTIN JJ
VANBROECKHOVEN C
TIMMERMAN V
Citation: P. Spoelders et al., MOLECULAR-GENETIC ANALYSIS OF CHARCOT-MARIE-TOOTH NEUROPATHY TYPE-2 (CMT2) FAMILIES WITH CHROMOSOME 1P35-36 AND 3Q13-22 MARKERS, Archives of physiology and biochemistry, 104(3), 1996, pp. 51-51
Authors:
VILLANOVA M
MALANDRINI A
TOTI P
SALVESTRONI R
SIX J
MARTIN JJ
GUAZZI GC
Citation: M. Villanova et al., LOCALIZATION OF MEROSIN IN THE NORMAL HUMAN BRAIN - IMPLICATIONS FOR CONGENITAL MUSCULAR-DYSTROPHY WITH MEROSIN DEFICIENCY, Journal of submicroscopic cytology and pathology, 28(1), 1996, pp. 1-4
Authors:
DEJONGHE P
KROLS L
MICHALIK A
HAZAN J
SMEYERS G
LOFGREN A
WEISSENBACH J
MARTIN JJ
VANBROECKHOVEN C
Citation: P. Dejonghe et al., PURE FAMILIAL SPASTIC PARAPLEGIA - CLINICAL AND GENETIC-ANALYSIS OF 9BELGIAN PEDIGREES, European journal of human genetics, 4(5), 1996, pp. 260-266
Authors:
TIMMERMAN V
DEJONGHE P
SIMOKOVIC S
LOFGREN A
BEUTEN J
NELIS E
CEUTERICK C
MARTIN JJ
VANBROECKHOVEN C
Citation: V. Timmerman et al., DISTAL HEREDITARY MOTOR NEUROPATHY TYPE-II (DISTAL HMN-II) - MAPPING OF A LOCUS TO CHROMOSOME 12Q24, Human molecular genetics, 5(7), 1996, pp. 1065-1069
Authors:
URENA A
DESALAZAR JMG
MARTIN JJ
QUINONES J
Citation: A. Urena et al., LATEST DEVELOPMENTS FOR MICROSTRUCTURAL AND CHEMICAL CHARACTERIZATIONOF DIFFUSION BONDING IN SUPERPLASTIC-8090 AL-LI ALLOYS, Journal of materials research, 11(1), 1996, pp. 63-71
Authors:
TIMMERMAN V
LOFGREN A
LEGUERN E
LIANG P
DEJONGHE P
MARTIN JJ
VERHALLE D
ROBBERECHT W
GOUIDER R
BRICE A
VANBROECKHOVEN C
Citation: V. Timmerman et al., MOLECULAR-GENETIC ANALYSIS OF THE 17P11.2 REGION IN PATIENTS WITH HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP), Human genetics, 97(1), 1996, pp. 26-34
Authors:
DEVOLDER I
TRUYEN L
VANGOETHEM J
VERCRUYSSEN A
MARTIN JJ
Citation: I. Devolder et al., TUBERCULOUS MENINGITIS IN IMMUNOCOMPETENT ADULTS - 2 CASES WITH A CLINICORADIOLOGICAL DISCUSSION, Clinical neurology and neurosurgery, 98(4), 1996, pp. 312-317
Authors:
KROLS L
MICHALIK A
DEJONGHE P
MARTIN JJ
VANBROECKHOVEN C
Citation: L. Krols et al., YAC CONTIG MAP OF THE CANDIDATE REGION FOR FAMILIAL SPASTIC PARAPLEGIA (SPG4) ON CHROMOSOME 2P21-]P14, Cytogenetics and cell genetics, 73(4), 1996, pp. 7-7
Authors:
BERWAERTS J
VERHELST J
VANDENBROUCKE M
ABS R
MARTIN JJ
MAHLER C
Citation: J. Berwaerts et al., THYROTOXIC PERIODIC PARALYSIS, AN UNUSUAL CAUSE OF HYPOKALEMIC PERIODIC PARALYSIS, Acta neurologica belgica, 96(4), 1996, pp. 301-306
Citation: Jj. Martin, HEREDITARY DISORDERS OF THE NERVOUS-SYSTEM - FROM ANATOMOCLINICAL STUDIES TO MOLECULAR-BIOLOGY, Acta neurologica belgica, 96(3), 1996, pp. 240-246
Citation: Bj. Cardinal et al., READABILITY OF WRITTEN INFORMED CONSENT FORMS USED IN EXERCISE AND SPORT PSYCHOLOGY RESEARCH, Research quarterly for exercise and sport, 67(3), 1996, pp. 360-362
Authors:
TIMMERMAN V
DEJONGHE P
SPOELDERS P
SIMOKOVIC S
LOFGREN A
NELIS E
VANCE J
MARTIN JJ
VANBROECKHOVEN C
Citation: V. Timmerman et al., LINKAGE AND MUTATION ANALYSIS OF CHARCOT-MARIE-TOOTH NEUROPATHY TYPE-2 FAMILIES WITH CHROMOSOMES 1P35-P36 AND XQ13, Neurology, 46(5), 1996, pp. 1311-1318
Authors:
MONSIEURS KG
VANBROECKHOVEN C
MARTIN JJ
DEHAENE I
HEYTENS LG
Citation: Kg. Monsieurs et al., MALIGNANT HYPERTHERMIA SUSCEPTIBILITY IN A PATIENT WITH CONCOMITANT MOTOR-NEURON DISEASE, Journal of the neurological sciences, 142(1-2), 1996, pp. 36-38
Citation: C. Ceuterick et Jj. Martin, SPORADIC EARLY ADULT-ONSET DISTAL MYOPATHY WITH RIMMED VACUOLES - IMMUNOHISTOCHEMISTRY AND ELECTRON-MICROSCOPY, Journal of the neurological sciences, 139(2), 1996, pp. 190-196
Authors:
CAMPBELL E
MARTIN JJ
BORDNER J
KLEINMAN EF
Citation: E. Campbell et al., ISOAROMATIZATION OF 4-ALKYLIDENE-3-OXO-1-CYCLOHEXENE-1-CARBOXYLATES -CONVENIENT SYNTHESIS OF METHYL 4-ALKYL-3-HYDROXYBENZOATES, Journal of organic chemistry, 61(14), 1996, pp. 4806-4809
Authors:
DECAESTECKER C
LOPES MBS
GORDOWER L
CRAS P
MARTIN JJ
KISS R
VANDENBERG S
SALMON I
Citation: C. Decaestecker et al., CHARACTERIZATION OF THE CHROMATIN PATTERN AND DNA-PLOIDY IN OLIGODENDROGLIOMAS, ASTROCYTOMAS, AND MIXED OLIGO-ASTROCYTOMAS, Journal of neuropathology and experimental neurology, 55(5), 1996, pp. 198-198
Authors:
ROBINSON RP
REITER LA
BARTH WE
CAMPETA AM
COOPER K
CRONIN BJ
DESTITO R
DONAHUE KM
FALKNER FC
FIESE EF
JOHNSON DL
KUPERMAN AV
LISTON TE
MALLOY D
MARTIN JJ
MITCHELL DY
RUSEK FW
SHAMBLIN SL
WRIGHT CF
Citation: Rp. Robinson et al., DISCOVERY OF THE HEMIFUMARATE AND (ALPHA-L-ALANYLOXY)METHYL ETHER AS PRODRUGS OF AN ANTIRHEUMATIC OXINDOLE - PRODRUGS FOR THE ENOLIC OH GROUP, Journal of medicinal chemistry, 39(1), 1996, pp. 10-18
Authors:
URENA A
DESALAZAR JMG
QUINONES J
MERINO S
MARTIN JJ
Citation: A. Urena et al., DIFFUSION BONDING OF AN ALUMINUM-LITHIUM ALLOY (AA8090) USING ALUMINUM-COPPER ALLOY INTERLAYERS .1. MICROSTRUCTURE, Journal of Materials Science, 31(3), 1996, pp. 807-817
Authors:
OOKAWARA T
DAVE V
WILLEMS P
MARTIN JJ
DEBARSY T
MATTHYS E
YOSHIDA A
Citation: T. Ookawara et al., RETARDED AND ABERRANT SPLICINGS CAUSED BY SINGLE EXON MUTATION IN A PHOSPHOGLYCERATE KINASE VARIANT, Archives of biochemistry and biophysics, 327(1), 1996, pp. 35-40