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Results: 1-25 | 26-27
Results: 1-25/27
OVERLOADED ENDOPLASMIC RETICULUM-GOLGI COMPARTMENTS, A POSSIBLE PATHOMECHANISM OF PERIPHERAL NEUROPATHIES CAUSED BY MUTATIONS OF THE PERIPHERAL MYELIN PROTEIN PMP22
Authors: DURSO D PRIOR R GREINERPETTER R GABREELSFESTEN AAWM MULLER HW
Citation: D. Durso et al., OVERLOADED ENDOPLASMIC RETICULUM-GOLGI COMPARTMENTS, A POSSIBLE PATHOMECHANISM OF PERIPHERAL NEUROPATHIES CAUSED BY MUTATIONS OF THE PERIPHERAL MYELIN PROTEIN PMP22, The Journal of neuroscience, 18(2), 1998, pp. 731-740
MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II EXPRESSION AND MACROPHAGE RESPONSES IN GENETICALLY PROVEN CHARCOT-MARIE-TOOTH TYPE-1 AND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES
Authors: STOLL G GABREELSFESTEN AAWM JANDER S MULLER HW HANEMANN CO
Citation: G. Stoll et al., MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II EXPRESSION AND MACROPHAGE RESPONSES IN GENETICALLY PROVEN CHARCOT-MARIE-TOOTH TYPE-1 AND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES, Muscle & nerve, 21(11), 1998, pp. 1419-1427
HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES - PHENOTYPICDIFFERENCES BETWEEN PATIENTS WITH THE COMMON DELETION AND A PMP22 FRAME-SHIFT MUTATION
Authors: LENSSEN PPA GABREELSFESTEN AAWM VALENTIJN LJ JONGEN PJH VANBEERSUM SEC VANENGELEN BGM VANWENSEN PJM BOLHUIS PA GABREELS EJM MARIMAN ECM
Citation: Ppa. Lenssen et al., HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES - PHENOTYPICDIFFERENCES BETWEEN PATIENTS WITH THE COMMON DELETION AND A PMP22 FRAME-SHIFT MUTATION, Brain (Print), 121, 1998, pp. 1451-1458
DIFFERENCES BETWEEN HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-2 AND CHRONIC IDIOPATHIC AXONAL NEUROPATHY - A CLINICAL AND ELECTROPHYSIOLOGICAL STUDY
Authors: TEUNISSEN LL NOTERMANS NC FRANSSEN H VANDERGRAAF Y OEY PL LINSSEN WHJP VANENGELEN BGM IPPEL PF VANDIJK GW GABREELSFESTEN AAWM WOKKE JHJ
Citation: Ll. Teunissen et al., DIFFERENCES BETWEEN HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-2 AND CHRONIC IDIOPATHIC AXONAL NEUROPATHY - A CLINICAL AND ELECTROPHYSIOLOGICAL STUDY, Brain, 120, 1997, pp. 955-962
SCHWANN-CELL DIFFERENTIATION IN CHARCOT-MARIE-TOOTH-DISEASE TYPE 1A (CMT1A) - NORMAL NUMBER OF MYELINATING SCHWANN-CELLS IN YOUNG CMT1A PATIENTS AND NEURAL CELL-ADHESION MOLECULE EXPRESSION IN ONION BULBS
Authors: HANEMANN CO GABREELSFESTEN AAWM STOLL G MULLER HW
Citation: Co. Hanemann et al., SCHWANN-CELL DIFFERENTIATION IN CHARCOT-MARIE-TOOTH-DISEASE TYPE 1A (CMT1A) - NORMAL NUMBER OF MYELINATING SCHWANN-CELLS IN YOUNG CMT1A PATIENTS AND NEURAL CELL-ADHESION MOLECULE EXPRESSION IN ONION BULBS, Acta Neuropathologica, 94(4), 1997, pp. 310-315
CLINICALLY DISTINCT CODON-69 MUTATIONS IN MAJOR MYELIN PROTEIN ZERO IN DEMYELINATING NEUROPATHIES
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
INHERITED DEMYELINATING PERIPHERAL NEUROPATHIES - RELATING MYELIN PACKING ABNORMALITIES TO PO MOLECULAR DEFECTS
Authors: KIRSCHNER DA SZUMOWSKI K GABREELSFESTEN AAWM HOOGENDIJK JE BOLHUIS PA
Citation: Da. Kirschner et al., INHERITED DEMYELINATING PERIPHERAL NEUROPATHIES - RELATING MYELIN PACKING ABNORMALITIES TO PO MOLECULAR DEFECTS, Journal of neuroscience research, 46(4), 1996, pp. 502-508
PERIPHERAL-NERVE ELONGATION BY LASER-DOPPLER FLOWMETRY-MONITORED EXPANSION - AN EXPERIMENTAL BASIS FOR FUTURE APPLICATION IN THE MANAGEMENTOF PERIPHERAL-NERVE DEFECTS
Authors: VANDERWEY LP POLDER TW STEGEMAN DF GABREELSFESTEN AAWM SPAUWEN PHM GABREELS FJM
Citation: Lp. Vanderwey et al., PERIPHERAL-NERVE ELONGATION BY LASER-DOPPLER FLOWMETRY-MONITORED EXPANSION - AN EXPERIMENTAL BASIS FOR FUTURE APPLICATION IN THE MANAGEMENTOF PERIPHERAL-NERVE DEFECTS, Plastic and reconstructive surgery, 97(3), 1996, pp. 568-576
2 DIVERGENT TYPES OF NERVE PATHOLOGY IN PATIENTS WITH DIFFERENT P-0 MUTATIONS IN CHARCOT-MARIE-TOOTH DISEASE
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
LOW-AFFINITY NGF RECEPTOR EXPRESSION IN CMT1A NERVE BIOPSIES OF DIFFERENT DISEASE STAGES
Authors: HANEMANN CO GABREELSFESTEN AAWM MULLER HW STOLL G
Citation: Co. Hanemann et al., LOW-AFFINITY NGF RECEPTOR EXPRESSION IN CMT1A NERVE BIOPSIES OF DIFFERENT DISEASE STAGES, Brain, 119, 1996, pp. 1461-1469
MITOCHONDRIAL CYTOPATHY PRESENTING AS HEREDITARY SENSORY NEUROPATHY WITH PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, ATAXIA AND FATAL MYOCLONIC EPILEPTIC STATUS
Authors: VANDOMBURG PHMF GABREELSFESTEN AAWM GABREELS FJM DECOO R RUITENBEEK W WESSELING P TERLAAK H
Citation: Phmf. Vandomburg et al., MITOCHONDRIAL CYTOPATHY PRESENTING AS HEREDITARY SENSORY NEUROPATHY WITH PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, ATAXIA AND FATAL MYOCLONIC EPILEPTIC STATUS, Brain, 119, 1996, pp. 997-1010
CONDUCTION-VELOCITY DISTRIBUTIONS COMPARED TO FIBER SIZE DISTRIBUTIONS IN NORMAL HUMAN SURAL NERVE
Authors: VANVEEN BK SCHELLENS RLLA STEGEMAN DF SCHOONHOVEN R GABREELSFESTEN AAWM
Citation: Bk. Vanveen et al., CONDUCTION-VELOCITY DISTRIBUTIONS COMPARED TO FIBER SIZE DISTRIBUTIONS IN NORMAL HUMAN SURAL NERVE, Muscle & nerve, 18(10), 1995, pp. 1121-1127
CLINICAL SYMPTOMS OF ADULT METACHROMATIC LEUKODYSTROPHY AND ARYLSULFATASE-A PSEUDODEFICIENCY
Authors: HAGEMAN ATM GABREELS FJM DEJONG JGN GABREELSFESTEN AAWM VANDENBERG CJMG VANOOST BA WEVERS RA
Citation: Atm. Hageman et al., CLINICAL SYMPTOMS OF ADULT METACHROMATIC LEUKODYSTROPHY AND ARYLSULFATASE-A PSEUDODEFICIENCY, Archives of neurology, 52(4), 1995, pp. 408-413
ELUCIDATION OF THE MOLECULAR DEFECT CAUSING A SEVERE TYPE OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES COMMON 1.5 MB DELETION IN CHROMOSOME-17P
Authors: MARIMAN ECM GABREELSFESTEN AAWM VANBEERSUM SEC VALENTIJN LJ BOLHUIS PA BAAS F ROPERS HH GABREELS FJM
Citation: Ecm. Mariman et al., ELUCIDATION OF THE MOLECULAR DEFECT CAUSING A SEVERE TYPE OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES COMMON 1.5 MB DELETION IN CHROMOSOME-17P, American journal of human genetics, 57(4), 1995, pp. 99-99
CHARCOT-MARIE-TOOTH DISEASE TYPE 1A - MORPHOLOGICAL PHENOTYPE OF THE 17P DUPLICATION VERSUS PMP22 POINT MUTATIONS
Authors: GABREELSFESTEN AAWM BOLHUIS PA HOOGENDIJK JE VALENTIJN LJ ESHUIS EJHM GABREELS FJM
Citation: Aawm. Gabreelsfesten et al., CHARCOT-MARIE-TOOTH DISEASE TYPE 1A - MORPHOLOGICAL PHENOTYPE OF THE 17P DUPLICATION VERSUS PMP22 POINT MUTATIONS, Acta Neuropathologica, 90(6), 1995, pp. 645-649
CONGENITAL MUSCULAR-DYSTROPHY AND SEVERE CENTRAL-NERVOUS-SYSTEM ATROPHY IN 2 SIBLINGS
Authors: LEYTEN QH BARTH PG GABREELS FJM RENKAWEK K RENIER WO GABREELSFESTEN AAWM TERLAAK HJ SMITS MG
Citation: Qh. Leyten et al., CONGENITAL MUSCULAR-DYSTROPHY AND SEVERE CENTRAL-NERVOUS-SYSTEM ATROPHY IN 2 SIBLINGS, Acta Neuropathologica, 90(6), 1995, pp. 650-656
PERIPHERAL-NERVE ELONGATION BY LASER-DOPPLER FLOWMETRY CONTROLLED EXPANSION - MORPHOLOGICAL ASPECTS
Authors: VANDERWEY LP GABREELSFESTEN AAWM MERKS MHJH POLDER TW STEGEMAN DF SPAUWEN PHM GABREELS FJM
Citation: Lp. Vanderwey et al., PERIPHERAL-NERVE ELONGATION BY LASER-DOPPLER FLOWMETRY CONTROLLED EXPANSION - MORPHOLOGICAL ASPECTS, Acta Neuropathologica, 89(2), 1995, pp. 166-171
THE STATUS OF HMSN TYPE-III
Authors: GABREELSFESTEN AAWM GABREELS FJM JENNEKENS FGI JANSSENVANKEMPEN TW
Citation: Aawm. Gabreelsfesten et al., THE STATUS OF HMSN TYPE-III, Neuromuscular disorders, 4(1), 1994, pp. 63-69
PREVALENCE OF THE 1.5-MB 17P DELETION IN FAMILIES WITH HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES
Authors: MARIMAN ECM GABREELSFESTEN AAWM VANBEERSUM SEC VALENTIJN LJ BAAS F BOLHUIS PA JONGEN PJH ROPERS HH GABREELS FJM
Citation: Ecm. Mariman et al., PREVALENCE OF THE 1.5-MB 17P DELETION IN FAMILIES WITH HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES, Annals of neurology, 36(4), 1994, pp. 650-655
EVIDENCE FOR GENETIC-HETEROGENEITY UNDERLYING HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES
Authors: MARIMAN ECM GABREELSFESTEN AAWM VANBEERSUM SEC JONGEN PJH VANDELOOIJ E BAAS F BOLHUIS PA ROPERS HH GABREELS FJM
Citation: Ecm. Mariman et al., EVIDENCE FOR GENETIC-HETEROGENEITY UNDERLYING HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES, Human genetics, 93(2), 1994, pp. 151-156
PERIPHERAL-NERVE ELONGATION BY LASER-DOPPLER FLOWMETRY CONTROLLED EXPANSION - FUNCTIONAL AND NEUROPHYSIOLOGICAL ASPECTS
Authors: VANDERWEY LP POLDER TW MERKS MHJH STEGEMAN DF VINGERHOETS DHM GABREELSFESTEN AAWM SPAUWEN PHM GABREELS FJM
Citation: Lp. Vanderwey et al., PERIPHERAL-NERVE ELONGATION BY LASER-DOPPLER FLOWMETRY CONTROLLED EXPANSION - FUNCTIONAL AND NEUROPHYSIOLOGICAL ASPECTS, Journal of the neurological sciences, 124(2), 1994, pp. 149-155
GENE FOR HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP) MAPS TO CHROMOSOME-17 AT OR CLOSE TO THE LOCUS FOR HMSN TYPE-1
Authors: MARIMAN ECM GABREELSFESTEN AAWM VANBEERSUM SEC JONGEN PJH ROPERS HH GABREELS FJM
Citation: Ecm. Mariman et al., GENE FOR HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP) MAPS TO CHROMOSOME-17 AT OR CLOSE TO THE LOCUS FOR HMSN TYPE-1, Human genetics, 92(1), 1993, pp. 87-90
HEREDITARY MOTOR AND SENSORY NEUROPATHIES PRESENT STATUS OF TYPE-I, TYPE-II AND TYPE-III
Authors: GABREELSFESTEN AAWM GABREELS FJM JENNEKENS FGI
Citation: Aawm. Gabreelsfesten et al., HEREDITARY MOTOR AND SENSORY NEUROPATHIES PRESENT STATUS OF TYPE-I, TYPE-II AND TYPE-III, Clinical neurology and neurosurgery, 95(2), 1993, pp. 93-107
A STATISTICAL APPROACH TO FIBER DIAMETER DISTRIBUTION IN HUMAN SURAL NERVE
Authors: SCHELLENS RLLA VANVEEN BK GABREELSFESTEN AAWM NOTERMANS SLH VANTHOF MA STEGEMAN DF
Citation: Rlla. Schellens et al., A STATISTICAL APPROACH TO FIBER DIAMETER DISTRIBUTION IN HUMAN SURAL NERVE, Muscle & nerve, 16(12), 1993, pp. 1342-1350
ALLELIC HETEROGENEITY IN HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-IA (CHARCOT-MARIE-TOOTH DISEASE TYPE-1A)
Authors: HOOGENDIJK JE JANSSEN EAM GABREELSFESTEN AAWM HENSELS GW JOOSTEN EMG GABREELS FJM ZORN I VALENTIJN LJ BAAS F DEVISSER BWO DEVISSER M BOLHUIS PA
Citation: Je. Hoogendijk et al., ALLELIC HETEROGENEITY IN HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-IA (CHARCOT-MARIE-TOOTH DISEASE TYPE-1A), Neurology, 43(5), 1993, pp. 1010-1015
Risultati: 1-25 | 26-27