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Results: 1-20 |
Results: 20
PURE MOTOR WEAKNESS AFTER RADIATION-THERA PY - 6 CASES
Authors: LALU T MERCIER B BIROUK N MAISONOBE T CATALA M LEFORESTIER N LEGER JM BOUCHE P
Citation: T. Lalu et al., PURE MOTOR WEAKNESS AFTER RADIATION-THERA PY - 6 CASES, Revue neurologique, 154(1), 1998, pp. 40-44
X-LINKED CHARCOT-MARIE-TOOTH-DISEASE WITH CONNEXIN-32 MUTATIONS - CLINICAL AND ELECTROPHYSIOLOGIC STUDY
Authors: BIROUK N LEGUERN E MAISONOBE T ROUGER H GOUIDER R TARDIEU S GUGENHEIM M ROUTON MC LEGER JM AGID Y BRICE A BOUCHE P
Citation: N. Birouk et al., X-LINKED CHARCOT-MARIE-TOOTH-DISEASE WITH CONNEXIN-32 MUTATIONS - CLINICAL AND ELECTROPHYSIOLOGIC STUDY, Neurology, 50(4), 1998, pp. 1074-1082
THE FIRST DE-NOVO MUTATION OF THE CONNEXIN-32 GENE ASSOCIATED WITH X-LINKED CHARCOT-MARIE-TOOTH-DISEASE
Authors: MEGGOUH F BENOMAR A ROUGER H TARDIEU S BIROUK N TASSIN J BARHOUMI C YAHYAOUI M CHKILI T BRICE A LEGUERN E
Citation: F. Meggouh et al., THE FIRST DE-NOVO MUTATION OF THE CONNEXIN-32 GENE ASSOCIATED WITH X-LINKED CHARCOT-MARIE-TOOTH-DISEASE, Journal of Medical Genetics, 35(3), 1998, pp. 251-252
CHARCOT-MARIE-TOOTH-DISEASE WITH INTERMEDIATE MOTOR-NERVE CONDUCTION VELOCITIES - CHARACTERIZATION OF 14 CX32 MUTATIONS IN 35 FAMILIES
Authors: ROUGER H LEGUERN E BIROUK N GOUIDER R TARDIEU S PLASSART E GUGENHEIM M VALLAT JM LOUBOUTIN JP BOUCHE P AGID E BRICE A
Citation: H. Rouger et al., CHARCOT-MARIE-TOOTH-DISEASE WITH INTERMEDIATE MOTOR-NERVE CONDUCTION VELOCITIES - CHARACTERIZATION OF 14 CX32 MUTATIONS IN 35 FAMILIES, Human mutation, 10(6), 1997, pp. 443-450
PATIENTS HOMOZYGOUS FOR THE 17P11.2 DUPLICATION IN CHARCOT-MARIE-TOOTH TYPE 1A DISEASE
Authors: LEGUERN E GOUIDER R MABIN D TARDIEU S BIROUK N PARENT P BOUCHE P BRICE A
Citation: E. Leguern et al., PATIENTS HOMOZYGOUS FOR THE 17P11.2 DUPLICATION IN CHARCOT-MARIE-TOOTH TYPE 1A DISEASE, Annals of neurology, 41(1), 1997, pp. 104-108
RECURRENT POLYRADICULONEUROPATHY WITH THE 17P11.2 DELETION
Authors: LEFORESTIER N LEGUERN E COULLIN P BIROUK N MAISONOBE T BRICE A LEGER JM BOUCHE P
Citation: N. Leforestier et al., RECURRENT POLYRADICULONEUROPATHY WITH THE 17P11.2 DELETION, Muscle & nerve, 20(9), 1997, pp. 1184-1186
CHARCOT-MARIE-TOOTH-DISEASE - ELECTROMYOG RAPHY IS STILL USEFUL IN DIAGNOSIS AND CLASSIFICATION
Authors: BIROUK N MAISONOBE T LEFORESTIER N GOUIDER R LEGER JM BOUCHE P
Citation: N. Birouk et al., CHARCOT-MARIE-TOOTH-DISEASE - ELECTROMYOG RAPHY IS STILL USEFUL IN DIAGNOSIS AND CLASSIFICATION, Revue neurologique, 153(12), 1997, pp. 727-736
MULTIFOCAL MOTOR NEUROPATHIES WITH CONDUC TION BLOCKS - 39 CASES
Authors: LEFORESTIER N CHASSANDE B MOULONGUET A MAISONOBE T SCHAEFFER S BIROUK N BAUMANN N ADAMS D LEGER JM MEININGER V SAID G BOUCHE P
Citation: N. Leforestier et al., MULTIFOCAL MOTOR NEUROPATHIES WITH CONDUC TION BLOCKS - 39 CASES, Revue neurologique, 153(10), 1997, pp. 579-586
HEREDITARY THERMOSENSITIVE NEUROPATHY - AN AUTOSOMAL-DOMINANT DISORDER OF THE PERIPHERAL NERVOUS-SYSTEM
Authors: MAGY L BIROUK N VALLAT JM GOUIDER R MAISONOBE T BOUCHE P LYONCAEN O FONTAINE B
Citation: L. Magy et al., HEREDITARY THERMOSENSITIVE NEUROPATHY - AN AUTOSOMAL-DOMINANT DISORDER OF THE PERIPHERAL NERVOUS-SYSTEM, Neurology, 48(6), 1997, pp. 1684-1690
A STUDY OF CANDIDATE GENES IN HEREDITARY THERMOSENSITIVE NEUROPATHY (HTN), AN AUTOSOMAL-DOMINANT DISORDER OF THE PERIPHERAL NERVOUS-SYSTEM
Authors: FONTAINE B MAGY L BIROUK N VALLAT JM GOUIDER R MAISONOBE T BOUCHE P LYONCAEN O
Citation: B. Fontaine et al., A STUDY OF CANDIDATE GENES IN HEREDITARY THERMOSENSITIVE NEUROPATHY (HTN), AN AUTOSOMAL-DOMINANT DISORDER OF THE PERIPHERAL NERVOUS-SYSTEM, Neurology, 48(3), 1997, pp. 5096-5096
SMN GENE ANALYSIS OF THE SPINAL FORM OF CHARCOT-MARIE-TOOTH-DISEASE
Authors: HANASH A LEGUERN E BIROUK N CLERMONT O POUGET J BOUCHE P MUNNICH A BRICE A MELKI J
Citation: A. Hanash et al., SMN GENE ANALYSIS OF THE SPINAL FORM OF CHARCOT-MARIE-TOOTH-DISEASE, Journal of Medical Genetics, 34(6), 1997, pp. 507-508
CHARCOT-MARIE-TOOTH DISEASE TYPE-1A WITH 17P11.2 DUPLICATION - CLINICAL AND ELECTROPHYSIOLOGICAL PHENOTYPE STUDY AND INFLUENCING DISEASE SEVERITY IN 119 CASES
Authors: BIROUK N GOUIDER R LEGUERN E GUGENHEIM M TARDIEU S MAISONOBE T LEFORESTIER N AGID Y BRICE A BOUCHE P
Citation: N. Birouk et al., CHARCOT-MARIE-TOOTH DISEASE TYPE-1A WITH 17P11.2 DUPLICATION - CLINICAL AND ELECTROPHYSIOLOGICAL PHENOTYPE STUDY AND INFLUENCING DISEASE SEVERITY IN 119 CASES, Brain, 120, 1997, pp. 813-823
CONSTANT REARRANGEMENT OF THE CMT1A-REP SEQUENCES IN HNPP PATIENTS WITH A DELETION IN CHROMOSOME 17P11.2 - A STUDY OF 34 UNRELATED CASES INCLUDING A DE-NOVO CASE OF MATERNAL ORIGIN
Authors: LEGUERN E GOUIDER R BIROUK N LOPES J ABBAS N GUGENHEIM M TARDIEU S RAVISE N LEGER JM VALLANT JM BOUCHE P AGID Y BRICE A
Citation: E. Leguern et al., CONSTANT REARRANGEMENT OF THE CMT1A-REP SEQUENCES IN HNPP PATIENTS WITH A DELETION IN CHROMOSOME 17P11.2 - A STUDY OF 34 UNRELATED CASES INCLUDING A DE-NOVO CASE OF MATERNAL ORIGIN, Neurology, 46(2), 1996, pp. 21003-21003
RECOMBINATION HOT-SPOT IN A 3.2-KB REGION OF THE CHARCOT-MARIE-TOOTH TYPE 1A REPEAT SEQUENCES - NEW TOOLS FOR MOLECULAR DIAGNOSIS OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES AND OF CHARCOT-MARIE-TOOTH TYPE 1A
Authors: LOPES J LEGUERN E GOUIDER R TARDIEU S ABBAS N BIROUK N GUGENHEIM M BOUCHE P AGID Y BRICE A ARNEBES MC BRICHET B CHAPON F CHAZOT G CLAVELOU P DESNUELLE C DIRAISON P DUBAS F GONNAUD PM HURTEVENT JF KUNTZER T LAGUENY A MABIN D MAYER M OCHSNER F OLLAGNONROMAN E POUGET J TABARAUD F VALLAT JM VANDENBERGHE A
Citation: J. Lopes et al., RECOMBINATION HOT-SPOT IN A 3.2-KB REGION OF THE CHARCOT-MARIE-TOOTH TYPE 1A REPEAT SEQUENCES - NEW TOOLS FOR MOLECULAR DIAGNOSIS OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES AND OF CHARCOT-MARIE-TOOTH TYPE 1A, American journal of human genetics, 58(6), 1996, pp. 1223-1230
HIGH-FREQUENCY OF MUTATIONS IN CODON098 OF THE PERIPHERAL MYELIN PROTEIN PO GENE IN 20 FRENCH CMT1 PATIENTS
Authors: ROUGER H LEGUERN E GOUIDER R TARDIEU S BIROUK N GUGENHEIM M BOUCHE P AGID Y BRICE A
Citation: H. Rouger et al., HIGH-FREQUENCY OF MUTATIONS IN CODON098 OF THE PERIPHERAL MYELIN PROTEIN PO GENE IN 20 FRENCH CMT1 PATIENTS, American journal of human genetics, 58(3), 1996, pp. 638-641
CONSTANT REARRANGEMENT OF THE CMT1A-REP SEQUENCES IN HNPP PATIENTS WITH A DELETION IN CHROMOSOME 17P11.2 - A STUDY OF 30 UNRELATED CASES
Authors: LEGUERN E GOUIDER R LOPES J ABBAS N GUGENHEIM M TARDIEU S RAVISE N LEGER JM VALLAT JM BOUCHE P AGID Y BRICE A ARNEBES MC BRICHET B BIROUK N CHAPON F CHAZOT G CLAVELOU P DESNUELLE C DIRAISON P DUBAS F GONNAUD PM HURTEVENT JF KUNTZER T LAGUENY A MABIN D OSHSNER F OLLAGNONROMAN E POUGET J TABERAUD F VANDENBERGHE A
Citation: E. Leguern et al., CONSTANT REARRANGEMENT OF THE CMT1A-REP SEQUENCES IN HNPP PATIENTS WITH A DELETION IN CHROMOSOME 17P11.2 - A STUDY OF 30 UNRELATED CASES, Human molecular genetics, 4(9), 1995, pp. 1673-1674
FAHRS-DISEASE AND DYSPARATHYROIDISM - 3 C ASE-REPORTS
Authors: ELMAGHRAOUI A BIROUK N ZAIM A SLASSI I YAHYAOUI M CHKILI T
Citation: A. Elmaghraoui et al., FAHRS-DISEASE AND DYSPARATHYROIDISM - 3 C ASE-REPORTS, La Presse medicale, 24(28), 1995, pp. 1301-1304
MIDDLE CEREBRAL-ARTERY OCCLUSION DUE TO HYDATID CYSTS OF MYOCARDIAL AND INTRAVENTRICULAR CAVITY CARDIAC ORIGIN - 2 CASES
Authors: BENOMAR A YAHYAOUI M BIROUK N VIDAILHET M CHKILI T
Citation: A. Benomar et al., MIDDLE CEREBRAL-ARTERY OCCLUSION DUE TO HYDATID CYSTS OF MYOCARDIAL AND INTRAVENTRICULAR CAVITY CARDIAC ORIGIN - 2 CASES, Stroke, 25(4), 1994, pp. 886-888
DERMATOMYOSITIS AND WILSONS-DISEASE
Authors: ELALAOUIFARIS M BENABDELJALIL M SLASSI I BOUTCHICHE M BIROUK N BELAIDI H SAIDI A CHKILI T
Citation: M. Elalaouifaris et al., DERMATOMYOSITIS AND WILSONS-DISEASE, Revue neurologique, 150(5), 1994, pp. 391-392
CARCINOMATOUS MENINGITIS AS THE 1ST MANIFESTATION OF DIGESTIVE-TRACT CANCER - 2 CASE-REPORTS WITH A REVIEW OF THE LITERATURE
Authors: BIROUK N ZEMRAG S BENOMAR A SAIDI A YAHYAOUI M CHKILI T
Citation: N. Birouk et al., CARCINOMATOUS MENINGITIS AS THE 1ST MANIFESTATION OF DIGESTIVE-TRACT CANCER - 2 CASE-REPORTS WITH A REVIEW OF THE LITERATURE, La Semaine des hopitaux de Paris, 69(18), 1993, pp. 541-544
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