Authors:
LALIOTI MD
SCOTT HS
GENTON P
GRID D
OUAZZANI R
MRABET A
IBRAHIM S
GOUIDER R
DRAVET C
CHKILI T
BOTTANI A
BURESI C
MALAFOSSE A
ANTONARAKIS SE
Citation: Md. Lalioti et al., A PCR AMPLIFICATION METHOD REVEALS INSTABILITY OF THE DODECAMER REPEAT IN PROGRESSIVE MYOCLONUS EPILEPSY (EPM1) AND NO CORRELATION BETWEEN THE SIZE OF THE REPEAT AND AGE AT ONSET, American journal of human genetics, 62(4), 1998, pp. 842-847
Authors:
LALIOTI MD
SCOTT HS
GENTON P
GRID D
OUAZZANI R
MRABET A
IBRAHIM S
GOUIDER R
DRAVET C
CHKILI T
BOTTANI A
BURESI C
MALAFOSSE A
ANTONARAKIS SE
Citation: Md. Lalioti et al., THE EXPANDED DODECAMER REPEAT IN PROGRESSIVE MYOCLONUS EPILEPSY (EPM1) IS UNSTABLE, SHOWS NO CORRELATION WITH AGE-OF-ONSET, AND RESULTS IN REDUCED EXPRESSION OF REPORTER GENES IN-VITRO, European journal of human genetics, 6, 1998, pp. 4166-4166
Authors:
PAOLONIGIACOBINO A
BURESI C
FENTON B
PREISIG M
GOLAZ J
GUIMON J
FERRERO F
MALAFOSSE A
Citation: A. Paolonigiacobino et al., PRELIMINARY-RESULTS OF AN ASSOCIATION STUDY BETWEEN THE TRYPTOPHAN-HYDROXYLASE GENE AND MANIAC DEPRESSIVE-ILLNESS IN A SWISS SAMPLE, European journal of human genetics, 6, 1998, pp. 4178-4178
Authors:
GOMEZGARRE P
ANTA B
CASTROGAGO M
LINDHOUT D
TASSINARI CA
MICHELUCCI R
MALAFOSSE A
TOPCU M
GRID D
DRAVET C
SERRATOSA J
Citation: P. Gomezgarre et al., REDUCTION OF THE LAFORA-DISEASE CANDIDATE GENE REGION TO A 2 CM INTERVAL IN CHROMOSOME 6Q24 AND EVIDENCE FOR GENETIC-HETEROGENEITY, European journal of human genetics, 6, 1998, pp. 4198-4198
Authors:
AGULHON C
KOBETZ A
BLANCHET P
SARDA P
BIANCALANA V
SITTLER A
MALAFOSSE A
ABITHOL M
Citation: C. Agulhon et al., EXPRESSION OF FMR1, FXR1, AND FXR2 GENES IN HUMAN PRENATAL TISSUES, European journal of neuroscience, 10, 1998, pp. 9814-9814
Authors:
KAREGE F
BOVIER P
STEPANIAN R
MALAFOSSE A
Citation: F. Karege et al., THE EFFECT OF CLINICAL OUTCOME ON PLATELET G-PROTEINS OF MAJOR DEPRESSED-PATIENTS, European neuropsychopharmacology, 8(2), 1998, pp. 89-94
Authors:
MOULARD B
SALACHAS F
CHASSANDE B
BRIOLOTTI V
MEININGER V
MALAFOSSE A
CAMU W
Citation: B. Moulard et al., ASSOCIATION BETWEEN CENTROMERIC DELETIONS OF THE SMN GENE AND SPORADIC ADULT-ONSET LOWER MOTOR-NEURON DISEASE, Annals of neurology, 43(5), 1998, pp. 640-644
Citation: P. Franken et al., GENETIC-VARIATION IN EEG ACTIVITY DURING SLEEP IN INBRED MICE, American journal of physiology. Regulatory, integrative and comparative physiology, 44(4), 1998, pp. 1127-1137
Authors:
BOUKAFTANE Y
KHORIS J
MOULARD B
SALACHAS F
MEININGER V
MALAFOSSE A
CAMU W
ROULEAU GA
Citation: Y. Boukaftane et al., IDENTIFICATION OF 6 NOVEL SOD1 GENE-MUTATIONS IN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS, Canadian journal of neurological sciences, 25(3), 1998, pp. 192-196
Authors:
AGULHON C
CHARNAY Y
VALLET P
BERTRAND D
MALAFOSSE A
Citation: C. Agulhon et al., DISTRIBUTION OF MESSENGER-RNA FOR THE ALPHA-4 SUBUNIT OF THE NICOTINIC ACETYLCHOLINE-RECEPTOR IN THE HUMAN FETAL BRAIN, Molecular brain research, 58(1-2), 1998, pp. 123-131
Authors:
KAREGE F
LAMBERCY C
RUDOLPH W
SCHWALD M
MALAFOSSE A
Citation: F. Karege et al., IN-VITRO STUDY OF G-PROTEIN ACTIVATION BY S-35 GTP-GAMMA-S BINDING TOPLATELET MEMBRANE - EFFECTS OF DIFFERENT MODULATORS, Biogenic amines, 14(1), 1998, pp. 25-40
Authors:
BELLIVIER F
LEBOYER M
COURTET P
BURESI C
SAMOLYK D
MALLET J
ALLILAIRE JF
FEINGOLD J
MALAFOSSE A
Citation: F. Bellivier et al., ASSOCIATION BETWEEN THE TRYPTOPHAN-HYDROXYLASE GENE AND SUICIDAL-BEHAVIOR IN BIPOLAR PATIENTS, American journal of medical genetics, 81(6), 1998, pp. 512-513
Authors:
PAOLONIGIACOBINO A
COURTET P
BELLIVIER F
ABBAR M
LAMBERCY C
MOUTHON D
VESSAZ M
MALLET J
BOULANGER JP
LEBOYER M
MALAFOSSE A
BURESI C
Citation: A. Paolonigiacobino et al., STUDY OF TRYPTOPHANE HYDROXYLASE GENE (TPH) POLYMORPHISMS IN BIPOLAR PATIENTS (BP) AND SUICIDE ATTEMPTERS (SA), American journal of medical genetics, 81(6), 1998, pp. 512-512
Authors:
GOUIDER R
IBRAHIM S
FREDJ M
GARGOURI A
SAIDI H
OUEZZANI R
MALAFOSSE A
YAHIAOUI M
GRID D
MRABET A
Citation: R. Gouider et al., UNVERRICHT-LUNDBORG-DISEASE - CLINICAL AND ELECTROPHYSIOLOGICAL ASPECTS IN 19 NORTH-AFRICAN FAMILIES, Revue neurologique, 154(6-7), 1998, pp. 503-507
Authors:
BELLIVIER F
LEBOYER M
COURTET P
BURESI C
BEAUFILS B
SAMOLYK D
ALLILAIRE JF
FEINGOLD J
MALLET J
MALAFOSSE A
Citation: F. Bellivier et al., ASSOCIATION BETWEEN THE TRYPTOPHAN-HYDROXYLASE GENE AND MANIC-DEPRESSIVE ILLNESS, Archives of general psychiatry, 55(1), 1998, pp. 33-37
Authors:
MALAFOSSE A
LEBOYER M
DAMATO T
AMADEO S
ABBAR M
CAMPION D
CANSEIL O
CASTELNAU D
GHEYSEN F
GRANGER B
HENRIKSON B
POIRIER MF
SABATE O
SAMOLYK D
FEINGOLD J
MALLET J
Citation: A. Malafosse et al., MANIC-DEPRESSIVE ILLNESS AND TYROSINE-HYDROXYLASE GENE - LINKAGE HETEROGENEITY AND ASSOCIATION, Neurobiology of disease, 4(5), 1997, pp. 337-349
Authors:
GUIPPONI M
RIVIER F
VIGEVANO F
BECK C
CRESPEL A
ECHENNE B
LUCCHINI P
SEBASTIANELLI R
BALDYMOULINIER M
MALAFOSSE A
Citation: M. Guipponi et al., LINKAGE MAPPING OF BENIGN FAMILIAL INFANTILE CONVULSIONS (BFIC) TO CHROMOSOME 19Q, Human molecular genetics, 6(3), 1997, pp. 473-477
Authors:
WIDMER J
MOUTHON D
RAFFIN Y
CHOLLET D
HILLERET H
MALAFOSSE A
BOVIER P
Citation: J. Widmer et al., WEAK ASSOCIATION BETWEEN BLOOD SODIUM, POTASSIUM, AND CALCIUM AND INTENSITY OF SYMPTOMS IN MAJOR DEPRESSED-PATIENTS, Neuropsychobiology, 36(4), 1997, pp. 164-171
Authors:
BELLIVIER F
LEBOYER M
COURTET P
BURESI C
BEAUFILS B
SAMOLYK D
FEINGOLD J
ALLILAIRE JF
MALLET J
MALAFOSSE A
Citation: F. Bellivier et al., ASSOCIATION BETWEEN THE TRYPTOPHAN-HYDROXYLASE GENE AND MANIC-DEPRESSIVE ILLNESS, American journal of medical genetics, 74(6), 1997, pp. 642-642
Authors:
GUIPPONI M
THOMAS P
GIRARDREYDET C
FEINGOLD J
BALDYMOULINIER M
MALAFOSSE A
Citation: M. Guipponi et al., LACK OF ASSOCIATION BETWEEN JUVENILE MYOCLONIC EPILEPSY AND GABRA5 AND GABRB3 GENES, American journal of medical genetics, 74(2), 1997, pp. 150-153
Authors:
MOULARD B
CAMU W
MALAFOSSE A
BILLIARD M
BALDYMOULINIER M
Citation: B. Moulard et al., CLINICAL ANALYSIS OF FAMILIAL AMYOTROPHIC -LATERAL-SCLEROSIS - REVIEWOF LITERATURE, Revue neurologique, 153(5), 1997, pp. 314-324
Citation: M. Guipponi et al., A FOK1 POLYMORPHISM IN THE HUMAN NEURONAL NICOTINIC ACETYLCHOLINE-RECEPTOR ALPHA-4 SUBUNIT GENE, Clinical genetics, 51(1), 1997, pp. 78-79