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Results: 1-25 |
Results: 25
EVIDENCE FOR THE SEGREGATION OF 3 DIFFERENT MUTATED ALLELES OF THE THYROGLOBULIN GENE IN A BRAZILIAN FAMILY WITH CONGENITAL GOITER AND HYPOTHYROIDISM
Authors: TARGOVNIK HM FRECHTEL GD MENDIVE FM VONO J COCHAUX P VASSART G MEDEIROSNETO G
Citation: Hm. Targovnik et al., EVIDENCE FOR THE SEGREGATION OF 3 DIFFERENT MUTATED ALLELES OF THE THYROGLOBULIN GENE IN A BRAZILIAN FAMILY WITH CONGENITAL GOITER AND HYPOTHYROIDISM, Thyroid, 8(4), 1998, pp. 291-297
THE DELTA-CCR5 MUTATION CONFERRING PROTECTION AGAINST HIV-1 IN CAUCASIAN POPULATIONS HAS A SINGLE AND RECENT ORIGIN IN NORTHEASTERN EUROPE
Authors: LIBERT F COCHAUX P BECKMAN G SAMSON M AKSENOVA M CAO A CZEIZEL A CLAUSTRES M DELARUA C FERRARI M FERREC C GLOVER G GRINDE B GURAN S KUCINSKAS V LAVINHA J MERCIER B OGUR G PELTONEN L ROSATELLI C SCHWARTZ M SPITSYN V TIMAR L BECKMAN L PARMENTIER M VASSART G
Citation: F. Libert et al., THE DELTA-CCR5 MUTATION CONFERRING PROTECTION AGAINST HIV-1 IN CAUCASIAN POPULATIONS HAS A SINGLE AND RECENT ORIGIN IN NORTHEASTERN EUROPE, Human molecular genetics, 7(3), 1998, pp. 399-406
SUBCUTANEOUS PANNICULITIS-LIKE T-CELL LYMPHOMA - FURTHER EVIDENCE FORA DISTINCT NEOPLASM ORIGINATING FROM LARGE GRANULAR LYMPHOCYTES OF T NK PHENOTYPE/
Authors: DARGENT JL ROUFOSSE C DELVILLE JP KENTOS A DELPLACE J KORNREICH A COCHAUX P HILBERT P PRADIER O FEREMANS W
Citation: Jl. Dargent et al., SUBCUTANEOUS PANNICULITIS-LIKE T-CELL LYMPHOMA - FURTHER EVIDENCE FORA DISTINCT NEOPLASM ORIGINATING FROM LARGE GRANULAR LYMPHOCYTES OF T NK PHENOTYPE/, Journal of cutaneous pathology, 25(7), 1998, pp. 394-400
INDUCTION OF SPECIFIC T-CELL RESPONSES IN HIV-INFECTION
Authors: LEANDERSSON AC BRATT G HINKULA J GILLJAM G COCHAUX P SAMSON M SANDSTROM E WAHREN B
Citation: Ac. Leandersson et al., INDUCTION OF SPECIFIC T-CELL RESPONSES IN HIV-INFECTION, AIDS, 12(2), 1998, pp. 157-166
RELATIVE CONTRIBUTION OF KI-RAS GENE ANALYSIS AND BRUSH CYTOLOGY DURING ERCP FOR THE DIAGNOSIS OF BILIARY AND PANCREATIC DISEASES
Authors: VANLAETHEM JL BOURGEOIS V PARMA J DELHAYE M COCHAUX P VELU T DEVIERE J CREMER M
Citation: Jl. Vanlaethem et al., RELATIVE CONTRIBUTION OF KI-RAS GENE ANALYSIS AND BRUSH CYTOLOGY DURING ERCP FOR THE DIAGNOSIS OF BILIARY AND PANCREATIC DISEASES, Gastrointestinal endoscopy, 47(6), 1998, pp. 479-485
GEOGRAPHIC-DISTRIBUTION AND REGIONAL ORIGIN OF 272 CYSTIC-FIBROSIS INEUROPEAN POPULATIONS
Authors: ESTIVILL X BANCELLS C RAMOS C PIAZZA A CARBONARA A MASTELLA G BONIZZATO A CASTALDI G DALCAMO E FERRARI M GASPARINI P GUANTI G LEONI GB PIGNATTI PF RONCHETTO P SEIA M TORRICELLI F GOOSSENS M CHEVALIERPORST F BOZON D SIMONBOUY B FELDMANN D ELION J KAPLAN JC FEREC C CLAUSTRES M CLAVEL C PUCHELLE E LUNARDI J MATHIEU M SCHEFFER H HALLEY DJJ VANDENOUWELAND AMW TIJMENSEN ASLN CASALS T GIMENEZ FJ RAMOS L BENEYTO M BENITEZ J PALACIO A TUMMLER B BAUER I MEITINGER T CLAASS A LINDNER M SCHRODER E STUHRMANN M CASSIMAN J CUPPENS H COCHAUX P PONCIN J MESSIAN L BARANOV VS IVASCHENKO TE BAKAY M BAL J WITT M KANAVAKIS M TZETIS M ANTONIADI T LAVINHA J PACHECO P DUARTE A LOUREIRO P KALAYDJIEVA L ANGELICHEVA D JORDANOVA A SAVOV A EIKLID K HOLMBERG L SCHAEDEL C OZGUC M GOCMEN A ERDERN H LIECHTIGALLATI S NEMETI M FEKETE G KLAASSEN T SCHWARZ M SCHWARTZ M MACEK M MACEK M KREBSOVA A VAVROVA V KEREM B AVELIOVICH D FERAK V KADASI L KAYSEROVA H GLAVAC D RAVNIKGLAVAC M EFREMOV GD CANKIKLEIN N KERE J
Citation: X. Estivill et al., GEOGRAPHIC-DISTRIBUTION AND REGIONAL ORIGIN OF 272 CYSTIC-FIBROSIS INEUROPEAN POPULATIONS, Human mutation, 10(2), 1997, pp. 135-154
NATURE OF THE T-LYMPHOCYTES IN LYMPHOCYTE PREDOMINANCE HODGKINS-DISEASE
Authors: DARGENT JL SCHANDENE L KORNREICH A LESPAGNARD L COCHAUX P JAGODZINSKI R CAPEL P VELU T NEVE P
Citation: Jl. Dargent et al., NATURE OF THE T-LYMPHOCYTES IN LYMPHOCYTE PREDOMINANCE HODGKINS-DISEASE, Leukemia & lymphoma, 24(5-6), 1997, pp. 545-551
MORPHOLOGIC AND PHENOTYPIC CHANGES OF THE LEUKEMIC-CELLS IN A CASE OFMARGINAL ZONE B-CELL LYMPHOMA
Authors: DARGENT JL DELVILLE JP KORNREICH A PRADIER O COCHAUX P VELU T CAPEL P FEREMANS W NEVE P
Citation: Jl. Dargent et al., MORPHOLOGIC AND PHENOTYPIC CHANGES OF THE LEUKEMIC-CELLS IN A CASE OFMARGINAL ZONE B-CELL LYMPHOMA, Annals of hematology, 74(3), 1997, pp. 149-153
DISSEMINATED ANGIOSARCOMA PRESENTING AS A HEMOPHAGOCYTIC SYNDROME IN A RENAL-ALLOGRAFT RECIPIENT
Authors: DARGENT JL VERMYLEN P ABRAMOWICZ D LESPAGNARD L COCHAUX P CAPEL P VELU T VEREERSTRAETEN P HAOT J DEWOLFPEETERS C
Citation: Jl. Dargent et al., DISSEMINATED ANGIOSARCOMA PRESENTING AS A HEMOPHAGOCYTIC SYNDROME IN A RENAL-ALLOGRAFT RECIPIENT, Transplant international, 10(1), 1997, pp. 61-64
ETV6 IS THE TARGET OF CHROMOSOME 12P DELETIONS IN T(12-21) CHILDHOOD ACUTE LYMPHOCYTIC-LEUKEMIA
Authors: CAVE H CACHEUX V RAYNAUD S BRUNIE G BAKKUS M COCHAUX P PREUDHOMME C LAI JL VILMER E GRANDCHAMP B
Citation: H. Cave et al., ETV6 IS THE TARGET OF CHROMOSOME 12P DELETIONS IN T(12-21) CHILDHOOD ACUTE LYMPHOCYTIC-LEUKEMIA, Leukemia, 11(9), 1997, pp. 1459-1464
THROMBOPHILIA PROFILE IN SNEDDON-SYNDROME PATIENTS
Authors: SORLIN P BLECIC S ADLERFLIGEL F WIJNS W COCHAUX P CAPEL P
Citation: P. Sorlin et al., THROMBOPHILIA PROFILE IN SNEDDON-SYNDROME PATIENTS, Thrombosis and haemostasis, 1997, pp. 597-597
COAGULATION DISORDER IN SNEDDON-SYNDROME
Authors: BLECIC S ADFERFLIGEL F SORLIN P CAPEL P COCHAUX P WIJNS W HILDEBRAND J
Citation: S. Blecic et al., COAGULATION DISORDER IN SNEDDON-SYNDROME, Neurology, 48(3), 1997, pp. 61009-61009
DOES KI-RAS ANALYSIS DURING ERCP EFFECTIVELY IMPROVE THE DIAGNOSIS OFBILIARY AND PANCREATIC DISEASES
Authors: BOURGEOIS V VANLAETHEM JL PARMA J DELHAYE M COCHAUX P VELU T DEVIERE J CREMER M
Citation: V. Bourgeois et al., DOES KI-RAS ANALYSIS DURING ERCP EFFECTIVELY IMPROVE THE DIAGNOSIS OFBILIARY AND PANCREATIC DISEASES, Gastrointestinal endoscopy, 45(4), 1997, pp. 395-395
KI-RAS MUTATIONS IN PATIENTS WITH CHRONIC-PANCREATITIS - HIGH PREVALENCE BUT UNDETERMINED RELEVANCE
Authors: VANLAETHEM JL BOURGEOIS V DELHAYE M PARMA J COCHAUX P VELU T DEVIERE J CREMER M
Citation: Jl. Vanlaethem et al., KI-RAS MUTATIONS IN PATIENTS WITH CHRONIC-PANCREATITIS - HIGH PREVALENCE BUT UNDETERMINED RELEVANCE, Gastroenterology, 112(4), 1997, pp. 490-490
SLIGHT INSTABILITY OF A FMR-1 ALLELE OVER 3 GENERATIONS IN A FAMILY FROM THE GENERAL-POPULATION
Authors: ABRAMOWICZ MJ PARMA J COCHAUX P
Citation: Mj. Abramowicz et al., SLIGHT INSTABILITY OF A FMR-1 ALLELE OVER 3 GENERATIONS IN A FAMILY FROM THE GENERAL-POPULATION, American journal of medical genetics, 64(2), 1996, pp. 268-269
PERNICIOUS-ANEMIA AND HYPOPARATHYROIDISM IN A PATIENT WITH KEARNS-SAYRE SYNDROME WITH MITOCHONDRIAL-DNA DUPLICATION
Authors: ABRAMOWICZ MJ COCHAUX P COHEN LHF VAMOS E
Citation: Mj. Abramowicz et al., PERNICIOUS-ANEMIA AND HYPOPARATHYROIDISM IN A PATIENT WITH KEARNS-SAYRE SYNDROME WITH MITOCHONDRIAL-DNA DUPLICATION, Journal of inherited metabolic disease, 19(2), 1996, pp. 109-111
NEUROLOGICAL DISORDERS IN MEMBERS OF FAMILIES WITH LEBERS HEREDITARY OPTIC NEUROPATHY (LHON) CAUSED BY DIFFERENT MITOCHONDRIAL MUTATIONS
Authors: MEIRE FM VANCOSTER R COCHAUX P OBERMAIERKUSSER B CANDAELE C MARTIN JJ
Citation: Fm. Meire et al., NEUROLOGICAL DISORDERS IN MEMBERS OF FAMILIES WITH LEBERS HEREDITARY OPTIC NEUROPATHY (LHON) CAUSED BY DIFFERENT MITOCHONDRIAL MUTATIONS, Ophthalmic genetics, 16(3), 1995, pp. 119-126
EXPERIENCE WITH 1251 TRANSCERVICAL CHORIONIC VILLUS SAMPLINGS PERFORMED IN THE FIRST TRIMESTER BY A SINGLE TEAM OF OPERATORS
Authors: DONNER C SIMON P KARIOUN A DELNESTE D ABRAMOWICZ M COCHAUX P RODESCH F
Citation: C. Donner et al., EXPERIENCE WITH 1251 TRANSCERVICAL CHORIONIC VILLUS SAMPLINGS PERFORMED IN THE FIRST TRIMESTER BY A SINGLE TEAM OF OPERATORS, European journal of obstetrics, gynecology, and reproductive biology, 60(1), 1995, pp. 45-51
TRANSPLANTED SICKLE-CELL DISEASE PATIENTS WITH AUTOLOGOUS BONE-MARROWRECOVERY AFTER GRAFT FAILURE DEVELOP INCREASED LEVELS OF FETAL HEMOGLOBIN WHICH CORRECTS DISEASE SEVERITY
Authors: FERSTER A CORAZZA F VERTONGEN F BUJAN W DEVALCK C FONDU P COCHAUX P LAMBERMONT M KHALADJI Z SARIBAN E
Citation: A. Ferster et al., TRANSPLANTED SICKLE-CELL DISEASE PATIENTS WITH AUTOLOGOUS BONE-MARROWRECOVERY AFTER GRAFT FAILURE DEVELOP INCREASED LEVELS OF FETAL HEMOGLOBIN WHICH CORRECTS DISEASE SEVERITY, British Journal of Haematology, 90(4), 1995, pp. 804-808
ABSENCE OF EPSTEIN-BARR-VIRUS IN MEDULLARY CARCINOMA OF THE BREAST ASDEMONSTRATED BY IMMUNOPHENOTYPING, IN-SITU HYBRIDIZATION AND POLYMERASE CHAIN-REACTION
Authors: LESPAGNARD L COCHAUX P LARSIMONT D DEGEYTER M VELU T HEIMANN R
Citation: L. Lespagnard et al., ABSENCE OF EPSTEIN-BARR-VIRUS IN MEDULLARY CARCINOMA OF THE BREAST ASDEMONSTRATED BY IMMUNOPHENOTYPING, IN-SITU HYBRIDIZATION AND POLYMERASE CHAIN-REACTION, American journal of clinical pathology, 103(4), 1995, pp. 449-452
PROXIMAL DELETION OF CHROMOSOME-21 CONFIRMED BY IN-SITU HYBRIDIZATIONAND MOLECULAR STUDIES
Authors: COURTENS W PETERSEN MB NOEL JC FLAMENTDURAND J VANREGEMORTER N DELNESTE D COCHAUX P VERSCHRAEGENSPAE MR VANROY N SPELEMAN F KOENIG U VAMOS E
Citation: W. Courtens et al., PROXIMAL DELETION OF CHROMOSOME-21 CONFIRMED BY IN-SITU HYBRIDIZATIONAND MOLECULAR STUDIES, American journal of medical genetics, 51(3), 1994, pp. 260-265
BRIEF REPORT - CLONAL PROLIFERATION OF TYPE-2 HELPER T-CELLS IN A MANWITH THE HYPEREOSINOPHILIC SYNDROME
Authors: COGAN E SCHANDENE L CRUSIAUX A COCHAUX P VELU T GOLDMAN M
Citation: E. Cogan et al., BRIEF REPORT - CLONAL PROLIFERATION OF TYPE-2 HELPER T-CELLS IN A MANWITH THE HYPEREOSINOPHILIC SYNDROME, The New England journal of medicine, 330(8), 1994, pp. 535-538
FEATURES OF MTDNA MUTATION PATTERNS IN EUROPEAN PEDIGREES AND SPORADIC CASES WITH LEBER HEREDITARY OPTIC NEUROPATHY
Authors: OBERMAIERKUSSER B LORENZ B SCHUBRING S PAPROTTA A ZERRES K MEITINGER T MEIRE F COCHAUX P BLANKENAGEL A KOMMERELL G JAKSCH M GERBITZ KD
Citation: B. Obermaierkusser et al., FEATURES OF MTDNA MUTATION PATTERNS IN EUROPEAN PEDIGREES AND SPORADIC CASES WITH LEBER HEREDITARY OPTIC NEUROPATHY, American journal of human genetics, 55(5), 1994, pp. 1063-1066
SOMATIC MUTATIONS IN THE THYROTROPIN RECEPTOR GENE CAUSE HYPERFUNCTIONING THYROID ADENOMAS
Authors: PARMA J DUPREZ L VANSANDE J COCHAUX P GERVY C MOCKEL J DUMONT J VASSART G
Citation: J. Parma et al., SOMATIC MUTATIONS IN THE THYROTROPIN RECEPTOR GENE CAUSE HYPERFUNCTIONING THYROID ADENOMAS, Nature, 365(6447), 1993, pp. 649-651
A NONSENSE MUTATION CAUSES HUMAN HEREDITARY CONGENITAL GOITER WITH PREFERENTIAL PRODUCTION OF A 171-NUCLEOTIDE-DELETED THYROGLOBULIN RIBONUCLEIC-ACID MESSENGER
Authors: TARGOVNIK HM MEDEIROSNETO G VARELA V COCHAUX P WAJCHENBERG BL VASSART G
Citation: Hm. Targovnik et al., A NONSENSE MUTATION CAUSES HUMAN HEREDITARY CONGENITAL GOITER WITH PREFERENTIAL PRODUCTION OF A 171-NUCLEOTIDE-DELETED THYROGLOBULIN RIBONUCLEIC-ACID MESSENGER, The Journal of clinical endocrinology and metabolism, 77(1), 1993, pp. 210-215
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