Works matching IS 00778923 AND DT 1999 AND VI 883 AND IP 1

Results: 73

Prenatal Diagnosis of Charcot-Marie-Tooth Disease Type 1A.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 457, doi. 10.1111/j.1749-6632.1999.tb08609.x

By:

KASHORK, CATHERINE D.;
CHEN, KEN-SHIUNG;
LUPSKI, JAMES R.;
SHAFFER, LISA G.

Publication type:

Article

Mutation Testing in Charcot-Marie-Tooth Neuropathy.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 383, doi. 10.1111/j.1749-6632.1999.tb08599.x

By:

NICHOLSON, GARTH A.

Publication type:

Article

Phenotypic Manifestations in French-Canadian Population with Charcot-Marie-Tooth Disease Type 1A Associated with 17p11.2 Duplication.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 497, doi. 10.1111/j.1749-6632.1999.tb08620.x

By:

DUPRÉ, NICOLAS;
BOUCHARD, JEAN-PIERRE;
COSSETTE, LOUISE;
BRUNET, DENIS;
VANASSE, MICHEL;
LEMIEUX, BERNARD;
MATHON, GILLES;
PUYMIRAT, JACK

Publication type:

Article

Distal Hereditary Motor Neuronopathy of the Jerash Type.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 439, doi. 10.1111/j.1749-6632.1999.tb08604.x

By:

MIDDLETON, L. T.;
CHRISTODOULOU, K.;
MUBAIDIN, A.;
ZAMBA, E.;
TSINGIS, M.;
KYRIACOU, K.;
ABU-SHEIKH, S.;
KYRIAKIDES, T.;
NEOCLEOUS, V.;
GEORGIOU, D. M.;
EL-KHATEEB, M.;
AL-QUDAH, A.;
HORANY, K.

Publication type:

Article

The Biology of Chronically Denervated Schwann Cells.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 215, doi. 10.1111/j.1749-6632.1999.tb08584.x

By:

HALL, SUSAN M.

Publication type:

Article

P0- Cre Transgenic Mice for Inactivation of Adhesion Molecules in Schwann Cells.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 116, doi. 10.1111/j.1749-6632.1999.tb08574.x

By:

FELTRI, MARIA LAURA;
D'ANTONIO, MAURIZIO;
PREVITALI, STEFANO;
FASOLINI, MARINA;
MESSING, ALBEE;
WRABETZ, LAWRENCE

Publication type:

Article

Trembler as a Mouse Model of CMT1A?

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 262, doi. 10.1111/j.1749-6632.1999.tb08588.x

By:

GARBAY, BERTRAND;
SALLES, JEROME;
KNOLL, ANJA;
BOIRON-SARGUEIL, FRANÇOISE;
HEAPE, ANTHONY M.;
BONNET, JACQUES;
CASSAGNE, CLAUDE

Publication type:

Article

Introduction to the Third International Symposium on Charcot-Marie-Tooth Disorders.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. xiii, doi. 10.1111/j.1749-6632.1999.tb08559.x

By:

SHY, MICHAEL E.;
KAMHOLZ, JOHN;
LOVELACE, ROBERT E.

Publication type:

Article

P0-Deficient Knockout Mice as Tools to Understand Pathomechanisms in Charcot-Marie-Tooth 1B and P0-Related Déjérine-Sottas Syndrome.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 273, doi. 10.1111/j.1749-6632.1999.tb08589.x

By:

MARTINI, RUDOLF

Publication type:

Article

Human Nerve Pathology Caused by Different Mutational Mechanisms of the PMP22 Gene.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 336, doi. 10.1111/j.1749-6632.1999.tb08595.x

By:

GABREËLS-FESTEN, ANNEKE;
VAN DE WETERING, RUDI

Publication type:

Article

New Vistas on the Pathomechanism of Charcot-Marie-Tooth and Related Peripheral Neuropathies.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 152, doi. 10.1111/j.1749-6632.1999.tb08578.x

By:

MÜLLER, H. W.

Publication type:

Article

Historical Perspective of Defining Charcot-Marie-Tooth Type 1B.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 6, doi. 10.1111/j.1749-6632.1999.tb08561.x

By:

BIRD, THOMAS D.

Publication type:

Article

Regulation of Myelin-Specific Gene Expression: Relevance to CMT1.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 91, doi. 10.1111/j.1749-6632.1999.tb08572.x

By:

KAMHOLZ, JOHN;
AWATRAMANI, RAJ;
MENICHELLA, DANIELA;
JIANG, HUIYUAN;
XU, WENBO;
SHY, MICHAEL

Publication type:

Article

Schwann Cell-Derived Desert Hedgehog Signals Nerve Sheath Formation.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 196, doi. 10.1111/j.1749-6632.1999.tb08582.x

By:

MIRSKY, RHONA;
PARMANTIER, ERIC;
MCMAHON, ANDREW P.;
JESSEN, KRISTJAN R.

Publication type:

Article

Why Do Schwann Cells Survive in the Absence of Axons?

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 109, doi. 10.1111/j.1749-6632.1999.tb08573.x

By:

JESSEN, K. R.;
MIRSKY, R.

Publication type:

Article

Molecular Mechanisms for CMT1A Duplication and HNPP Deletion.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 22, doi. 10.1111/j.1749-6632.1999.tb08563.x

By:

BOERKOEL, C. F.;
INOUE, K.;
REITER, L. T.;
WARNER, L. E.;
LUPSKI, J. R.

Publication type:

Article

HMSN and HNPP: Laboratory Service Provision in the South West of England-Two Years' Experience.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 500, doi. 10.1111/j.1749-6632.1999.tb08621.x

By:

WILLIAMS, M. M.;
TYFIELD, L. A.;
JARDINE, P.;
LUNT, P. W.;
STEVENS, D. L.;
TURNPENNY, P. D.

Publication type:

Article

Overview of Charcot-Marie-Tooth Disease Type 1A.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 1, doi. 10.1111/j.1749-6632.1999.tb08560.x

By:

THOMAS, P. K.

Publication type:

Article

Schwann Cell-Axon Interactions in Charcot-Marie-Tooth Disease.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 77, doi. 10.1111/j.1749-6632.1999.tb08571.x

By:

GRIFFIN, JOHN W.;
SHEIKH, KAZIM

Publication type:

Article

Charcot-Marie-Tooth 1A: Heterozygous T118M Mutation over a CMT1A Duplication Has No Influence on the Phenotype.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 485, doi. 10.1111/j.1749-6632.1999.tb08617.x

By:

SEEMAN, P.;
MAZANEC, R.;
MARIKOVA, T.;
RAUTENSTRAUSS, B.

Publication type:

Article

Characterization of Targeted Connexin32-Deficient Mice: A Model for the Human Charcot-Marie-Tooth (X-Type) Inherited Disease.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 302, doi. 10.1111/j.1749-6632.1999.tb08592.x

By:

WILLECKE, KLAUS;
TEMME, ACHIM;
TEUBNER, BARBARA;
OTT, THOMAS

Publication type:

Article

Characteristics of Gap Junction Channels in Schwann Cells from Wild-Type and Connexin-Null Mice.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 533, doi. 10.1111/j.1749-6632.1999.tb08630.x

By:

ZHAO, SHUMIN;
FORT, ALFREDO;
SPRAY, DAVID C.

Publication type:

Article

Electrodiagnostic Findings in CMTX: A Disorder of the Schwann Cell and Peripheral Nerve Myelin.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 504, doi. 10.1111/j.1749-6632.1999.tb08622.x

By:

LEWIS, RICHARD A.;
SHY, MICHAEL E.

Publication type:

Article

A Unique Mutation in Connexin32 Associated with Severe, Early Onset CMTX in a Heterozygous Female.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 481, doi. 10.1111/j.1749-6632.1999.tb08616.x

By:

LIN, GRACE S.;
GLASS, JONATHAN D.;
SHUMAS, SUSAN;
SCHERER, STEVEN S.;
FISCHBECK, KENNETH H.

Publication type:

Article

Construction of a PAC Contig within the Distal Hereditary Motor Neuropathy Type II Candidate Region at 12q24.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 463, doi. 10.1111/j.1749-6632.1999.tb08611.x

By:

IROBI, JOY;
TIMMERMAN, VINCENT;
JONGHE, PETER;
VRIENDT, ELS;
VAN BROECKHOVEN, CHRISTINE;
BEUTEN, J.

Publication type:

Article

Altered Assembly of Gap Junction Channels Caused by COOH-Terminal Connexin32 Mutants of CMTX.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 526, doi. 10.1111/j.1749-6632.1999.tb08628.x

By:

BARRIO, LUIS C.;
CASTRO, CARMEN;
GÓMEZ-HERNANDEZ, JUAN M.

Publication type:

Article

Alterations in Nodes of Ranvier and Schmidt-Lanterman Incisures in Charcot-Marie-Tooth Neuropathies.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 508, doi. 10.1111/j.1749-6632.1999.tb08623.x

By:

SAHENK, ZARIFE;
MENDELL, JERRY R.

Publication type:

Article

A Second Family with Autosomal Dominant Burning Feet Syndrome.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 445, doi. 10.1111/j.1749-6632.1999.tb08606.x

By:

KUHLENBÄUMER, G.;
YOUNG, P.;
KIEFER, R.;
TIMMERMAN, V.;
WANG, J.-F.;
SCHROEDER, J. M.;
WEIS, J.;
RINGELSTEIN, E. B.;
VAN BROECKHOVEN, C.;
STOEGBAUER, F.

Publication type:

Article

Trophic Factors in Neuron-Schwann Cell Interactions.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 427, doi. 10.1111/j.1749-6632.1999.tb08603.x

By:

FRIEDMAN, H.C. HYMAN;
AGUAYO, A. J.;
BRAY, G. M.

Publication type:

Article

Transgenic Mouse Models of CMT1A and HNPP.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 247, doi. 10.1111/j.1749-6632.1999.tb08586.x

By:

SUTER, UELI;
NAVE, KLAUS-ARMIN

Publication type:

Article

Neurofibromin, the Neurofibromatosis Type 1 Ras-GAP, Is Required for Appropriate P0 Expression and Myelination.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 203, doi. 10.1111/j.1749-6632.1999.tb08583.x

By:

ROSENBAUM, THORSTEN;
KIM, HAESUN A.;
BOISSY, YING L.;
LING, BO;
RATNER, NANCY

Publication type:

Article

Distal Hereditary Motor Neuronopathy of the Jerash Type.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 65, doi. 10.1111/j.1749-6632.1999.tb08569.x

By:

MIDDLETON, L. T.;
CHRISTODOULOU, K.;
MUBAIDIN, A.;
ZAMBA, E.;
TSINGIS, M.;
KYRIACOU, K.;
ABU-SHEIKH, S.;
KYRIAKIDES, T.;
NEOCLEOUS, V.;
GEORGIOU, D. M.;
EL-KHATEEB, M.;
AL-QUDAN, A.;
HORANY, K.

Publication type:

Article

The 'CMT Rat': Peripheral Neuropathy and Dysmyelination Caused by Transgenic Overexpression of PMP22.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 254, doi. 10.1111/j.1749-6632.1999.tb08587.x

By:

NIEMANN, STEPHAN;
SEREDA, MICHAEL W.;
ROSSNER, MORITZ;
STEWART, HELEN;
SUTER, UELI;
MEINCK, HANS-MICHAEL;
GRIFFITHS, IAN R.;
NAVE, KLAUS-ARMIN

Publication type:

Article

Peripheral Nerve Dysmyelination Due to P0 Glycoprotein Overexpression Is Dose-Dependent.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 294, doi. 10.1111/j.1749-6632.1999.tb08591.x

By:

QUATTRINI, ANGELO;
FELTRI, MARIA LAURA;
PREVITALI, STEFANO;
FASOLINI, MARINA;
MESSING, ALBEE;
WRABETZ, LAWRENCE

Publication type:

Article

Hereditary Motor and Sensory Neuropathy with Proximal Dominant Involvement: Clinical, Pathological, and Genetic Features.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 449, doi. 10.1111/j.1749-6632.1999.tb08607.x

By:

NAKAGAWA, MASANORI;
TAKASHIMA, HIROSHI;
SUEHARA, MASAHITO;
SAITO, MINEKI;
SAITO, AKIKO;
KANZATO, NAOMI;
MATSUZAKI, TOSHIO;
HIRATA, KEIKO;
IZUMO, SHUJI;
TERWILLIGER, JOSEPH D.;
OSAME, MITSUHIRO

Publication type:

Article

Overview of Hereditary Neuropathy with Liability to Pressure Palsies.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 14, doi. 10.1111/j.1749-6632.1999.tb08562.x

By:

CHANCE, PHILIP F.

Publication type:

Article

Overcoming Cellular Immunity to Prolong Adenoviral-Mediated Gene Expression in Sciatic Nerve.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 397, doi. 10.1111/j.1749-6632.1999.tb08601.x

By:

JANI, AGNES;
MENICHELLA, DANIELA;
JIANG, HUIYUAN;
CHBIHI, TAIBI;
ACSADI, GYULA;
KAMHOLZ, JOHN;
SHY, MICHAEL E.

Publication type:

Article

X-linked Charcot-Marie-Tooth Disease and Connexin32.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 36, doi. 10.1111/j.1749-6632.1999.tb08564.x

By:

FISCHBECK, KENNETH H.;
ABEL, ANNETTE;
LIN, GRACE S.;
SCHERER, STEVEN S.

Publication type:

Article

Autosomal Recessive Hereditary Motor and Sensory Neuropathy with Focally Folded Myelin Sheaths (CMT4B).

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 47, doi. 10.1111/j.1749-6632.1999.tb08566.x

By:

GAMBARDELLA, ANTONIO;
BONO, FRANCESCO;
MUGLIA, MARIELLA;
VALENTINO, PAOLA;
QUATTRONE, ALDO

Publication type:

Article

A Clinical Review of Charcot-Marie-Tooth.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 69, doi. 10.1111/j.1749-6632.1999.tb08570.x

By:

GARCIA, CARLOS A.

Publication type:

Article

Schwann Cell Apoptosis during Cell-Mediated Demyelination.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 518, doi. 10.1111/j.1749-6632.1999.tb08625.x

By:

CONTI, G.;
SCARPINI, E.;
ROSTAMI, A.;
LIVRAGHI, S.;
CLERICI, R.;
PICCIO, L.;
SIGLIENTI, I.;
BARON, P. L.;
PLEASURE, D.;
SCARLATO, G.

Publication type:

Article

Abnormal Schwann Cell-Axon Interactions in CMT Neuropathies: The Effects of Mutant Schwann Cells on the Axonal Cytoskeleton and Regeneration-Associated Myelination.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 415, doi. 10.1111/j.1749-6632.1999.tb08602.x

By:

SAHENK, ZARIFE

Publication type:

Article

A Family with Friedreich Ataxia and Onion-Bulb Formations at Sural Nerve Biopsy.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 466, doi. 10.1111/j.1749-6632.1999.tb08612.x

By:

BARREIRA, A. A.;
MARQUES, W.;
SWEENEY, M. G.;
DAVIS, M. B.;
CHIMELLI, L.;
PAÇÓ-LARSON, M. L.;
WOOD, N. W.

Publication type:

Article

Molecular Diagnostic Testing in Charcot-Marie-Tooth Disease and Related Disorders: Approaches and Results.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 389, doi. 10.1111/j.1749-6632.1999.tb08600.x

By:

JONGHE, P.;
NELIS, E.;
TIMMERMAN, V.;
LÖFGREN, A.;
MARTIN, J-J.;
VAN BROECKHOVEN, C.

Publication type:

Article

Heterozygous Null Mutation in the P0 Gene Associated with Mild Charcot-Marie-Tooth Disease.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 477, doi. 10.1111/j.1749-6632.1999.tb08615.x

By:

PAREYSON, D.;
MENICHELLA, D.;
BOTTI, S.;
SGHIRLANZONI, A.;
FALLICA, E.;
MORA, M.;
CIANO, C.;
SHY, M. E.;
TARONI, F.

Publication type:

Article

The Anatomy and Cell Biology of Peripheral Myelin Protein-22.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 143, doi. 10.1111/j.1749-6632.1999.tb08577.x

By:

SNIPES, G. JACKSON;
ORFALI, WAYEL;
FRASER, ANDREW;
DICKSON, KATHLEEN;
COLBY, JOSHUA

Publication type:

Article

Distal Hereditary Motor Neuropathy Type II (Distal HMN Type II): Phenotype and Molecular Genetics.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 60, doi. 10.1111/j.1749-6632.1999.tb08568.x

By:

TIMMERMAN, V.;
BEUTEN, J.;
IROBI, J.;
JONGHE, P.;
MARTIN, J.-J.;
VAN BROECKHOVEN, C.

Publication type:

Article

Charcot-Marie-Tooth Disease Type 2.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 42, doi. 10.1111/j.1749-6632.1999.tb08565.x

By:

VANCE, JEFFERY M.

Publication type:

Article

Human Schwann Cell Proliferation and IL-6 Production following TNF-α Stimulation in Vitro.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 520, doi. 10.1111/j.1749-6632.1999.tb08626.x

By:

SCARPINI, E.;
CONTI, G. C.;
BUSSINI, S.;
CLERICI, R.;
SIGLIENTI, I.;
PICCIO, L.;
POL, A.;
BARON, P. L.;
SCARLATO, G.

Publication type:

Article

Induction of Myelin Gene Expression in Murine Schwann Cells in Primary Culture and in a Schwann Cell Line.

Published in:

Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 513, doi. 10.1111/j.1749-6632.1999.tb08624.x

By:

NICHOLSON, S. M.;
GOMÈS, D.;
BARON-VAN EVERCOOREN, A.;
BRUZZONE, R.

Publication type:

Article