Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where authors phrase all words ' Amiel, J' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 77 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Garcia, G; Chevallier, D; Amiel, J; Toubol, J; Michiels, JF
      Prospective study comparing ultrasound-guided transrectal biopsy and finger-guided transperineal biopsy in the diagnosis of prostate cancer

      PROGRES EN UROLOGIE
    2. Fuchs, S; Amiel, J; Claudel, S; Lyonnet, S; Corvol, P; Pinet, F
      Functional characterization of three mutations of the endothelin B receptor gene in patients with Hirschsprung's disease: Evidence for selective lossof G(i) coupling

      MOLECULAR MEDICINE
    3. Amiel, J; Bougeard, G; Francannet, C; Raclin, V; Munnich, A; Lyonnet, S; Frebourg, T
      TP63 gene mutation in ADULT syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    4. Colleaux, L; Rio, M; Heuertz, S; Moindrault, S; Turleau, C; Ozilou, C; Gosset, P; Raoult, O; Lyonnet, S; Cormier-Daire, V; Amiel, J; Le Merrer, M; Picq, M; de Blois, MC; Prieur, M; Romana, S; Cornelis, F; Vekemans, M; Munnich, A
      A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation

      EUROPEAN JOURNAL OF HUMAN GENETICS
    5. Mahieu-Caputo, D; Sonigo, P; Amiel, J; Simon, I; Aubry, MC; Lemerrer, M; Delezoide, AL; Gigarel, N; Dommergues, M; Dumez, Y
      Prenatal diagnosis of sporadic Apert syndrome: A sequential diagnostic approach combining three-dimensional computed tomography and molecular biology

      FETAL DIAGNOSIS AND THERAPY
    6. Holder-Espinasse, M; de Blois, MC; Faivre, L; Romana, S; Uteza, Y; Munnich, A; Lyonnet, S; Cormier-Daire, V; Amiel, J
      Absent lacrimal ducts, distichiasis, dysmorphic features, and brachydactyly: a case report

      CLINICAL DYSMORPHOLOGY
    7. Amiel, J; Faivre, L; Marianowskl, R; Bonnet, D; Couly, G; Manach, Y; Le Merrer, M; Cormier-Daire, V; Munnich, A; Lyonnet, S
      Hypertelorism-Microtia-Clefting Syndrome (Bixler syndrome): report of two unrelated cases

      CLINICAL DYSMORPHOLOGY
    8. Amiel, J; Gigarel, N; Benacki, A; Benit, P; Valnot, I; Parfait, W; Von Kleist-Retzow, JC; Raclin, V; Hadj-Rabia, S; Dumez, Y; Rustin, P; Bonnefont, JP; Munnich, A; Rotig, A
      Prenatal diagnosis of respiratory chain deficiency by direct mutation screening

      PRENATAL DIAGNOSIS
    9. Dureau, P; Attie-Bitach, T; Salomon, R; Bettembourg, O; Amiel, J; Uteza, Y; Dufier, JL
      Renal coloboma syndrome

      OPHTHALMOLOGY
    10. Amiel, J; Attie-Bitach, T; Marianowski, R; Cormier-Daire, V; Abadie, V; Bonnet, D; Gonzales, M; Chemouny, S; Brunelle, F; Munnich, A; Manach, Y; Lyonnet, S
      Temporal bone anomaly proposed as a major criteria for diagnosis of CHARGEsyndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    11. Salomon, R; Tellier, AL; Attie-Bitach, T; Amiel, J; Vekemans, M; Lyonnet, S; Dureau, P; Niaudet, P; Gubler, MC; Broyer, M
      PAX2 mutations in oligomeganephronia

      KIDNEY INTERNATIONAL
    12. Holder-Espinasse, M; Abadie, V; Cormier-Daire, V; Beyler, C; Manach, Y; Munnich, A; Lyonnet, S; Couly, G; Amiel, J
      Pierre Robin sequence: A series of 117 consecutive cases

      JOURNAL OF PEDIATRICS
    13. Imessaoudene, B; Bonnefont, JP; Royer, G; Cormier-Daire, V; Lyonnet, S; Lyon, G; Munnich, A; Amiel, J
      MECP2 mutation in non-fatal, non-progressive encephalopathy in a male

      JOURNAL OF MEDICAL GENETICS
    14. Amiel, J; Lyonnet, S
      Hirschsprung disease, associated syndromes, and genetics: a review

      JOURNAL OF MEDICAL GENETICS
    15. Cattan, I; Rochet, N; Mazeau, C; Zanghellini, E; Mari, B; Chauzy, C; de Novion, HS; Amiel, J; Lagrange, JL; Rossi, B; Gioanni, J
      Establishment of two new human bladder carcinoma cell lines, CAL 29 and CAL 185. Comparative study of cell scattering and epithelial to mesenchyme transition induced by growth factors

      BRITISH JOURNAL OF CANCER
    16. Amiel, J; Espinosa-Parrilla, Y; Steffann, J; Gosset, P; Pelet, A; Prieur, M; Boute, O; Choiset, A; Lacombe, D; Philip, N; Le Merrer, M; Tanaka, H; Till, M; Touraine, R; Toutain, A; Vekemans, M; Munnich, A; Lyonnet, S
      Large-scale deletions and SMADIP1 truncating mutations in syndromic hirschsprung disease with involvement of midline structures

      AMERICAN JOURNAL OF HUMAN GENETICS
    17. Amiel, J; Audollent, S; Joly, D; Dureau, P; Salomon, R; Tellier, AL; Auge, J; Bouissou, F; Antignac, C; Gubler, MC; Eccles, MR; Munnich, A; Vekemans, M; Lyonnet, S; Attie-Bitach, T
      PAX2 mutations in renal-coloboma syndrome: mutational hotspot and germlinemosaicism

      EUROPEAN JOURNAL OF HUMAN GENETICS
    18. Gagnadoux, MF; Attie, T; Amiel, J; Gigarel, N; Bonnefont, JP; Munnich, A; Gubler, MC; Antignac, C
      Prenatal diagnosis in autosomal recessive polycystic kidney disease

      ARCHIVES DE PEDIATRIE
    19. Chretiennot, C; Andreu, J; Simon, I; Amiel, J; Zerah, M
      Radiological quiz of the month - Klippel-Feil syndrome

      ARCHIVES DE PEDIATRIE
    20. Abadie, V; Wiener-Vacher, S; Morisseau-Durand, MP; Poree, C; Amiel, J; Amanou, L; Peigne, C; Lyonnet, S; Manac'h, Y
      Vestibular anomalies in CHARGE syndrome: investigations on and consequences for postural development

      EUROPEAN JOURNAL OF PEDIATRICS
    21. Faivre, L; Cormier-Daire, V; Chretien, D; von Kleist-Retzow, JC; Amiel, J; Dommergues, M; Saudubray, JM; Dumez, Y; Rotig, A; Rustin, P; Munnich, A
      Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiency

      PRENATAL DIAGNOSIS
    22. Tellier, AL; Amiel, J; Delezoide, AL; Audollent, S; Auge, J; Esnault, D; Encha-Razavi, F; Munnich, A; Lyonnet, S; Vekemans, M; Attie-Bitach, T
      Expression of the PAX2 gene in human embryos and exclusion in the CHARGE syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    23. Sanlaville, D; Aubry, MC; Dumez, Y; Nolen, MC; Amiel, J; Pinson, MP; Lyonnet, S; Munnich, A; Vekemans, M; Morichon-Delvallez, N
      Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow up

      JOURNAL OF MEDICAL GENETICS
    24. Cormier-Daire, V; Amiel, J; Vuillaumier-Barrot, S; Tan, J; Durand, G; Munnich, A; Le Merrer, M; Seta, N
      Congenital disorders of glycosylation IIa cause growth retardation, mentalretardation, and facial dysmorphism

      JOURNAL OF MEDICAL GENETICS
    25. Valnot, I; Osmond, S; Gigarel, N; Mehaye, B; Amiel, J; Cormier-Daire, V; Munnich, A; Bonnefont, JP; Rustin, P; Rotig, A
      Mutations of the SCO1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathy

      AMERICAN JOURNAL OF HUMAN GENETICS
    26. Amiel, J; de Lonlay, P; Francannet, C; Picard, A; Bruel, H; Rabier, D; Le Merrer, M; Verhoeven, N; Jakobs, C; Lyonnet, S; Munnich, A
      Facial anomalies in D-2-hydroxyglutaric aciduria

      AMERICAN JOURNAL OF MEDICAL GENETICS
    27. van der Knaap, MS; Jakobs, C; Hoffmann, GF; Duran, M; Muntau, AC; Schweitzer, S; Kelley, RI; Parrot-Roulaud, F; Amiel, J; De Lonlay, P; Rabier, D; Eeg-Olofsson, O
      D-2-hydroxyglutaric aciduria: Further clinical delineation

      JOURNAL OF INHERITED METABOLIC DISEASE
    28. Amiel, J; Cormier-Daire, V; Journeau, P; Mussat, P; Munnich, A; Lyonnet, S
      Epiphyseal, vertebral, and ear (EVE) dysplasia: a new syndrome?

      JOURNAL OF MEDICAL GENETICS
    29. Bonnet, D; Fermont, L; Kachaner, J; Sidi, D; Amiel, J; Lyonnet, S; Munnich, A
      Tricuspid atresia and conotruncal malformations in five families

      JOURNAL OF MEDICAL GENETICS
    30. Manouvrier-Hanu, S; Amiel, J; Jacquot, S; Merienne, K; Moerman, A; Coeslier, A; Labarriere, F; Vallee, L; Croquette, MF; Hanauer, A
      Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndrome

      JOURNAL OF MEDICAL GENETICS
    31. Picard, C; Couderc, S; Skojaei, T; Salomon, R; de Lonlay, P; Le Merrer, M; Munnich, A; Lyonnet, S; Amiel, J
      Scalp-ear-nipple (Finlay-Marks) syndrome: a familial case with renal involvement

      CLINICAL GENETICS
    32. Kara-Mostefa, A; Raoul, O; Lyonnet, S; Amiel, J; Munnich, A; Vekemans, M; Magnier, S; Ossareh, B; Bonnefont, JP
      Recurrent Williams-Beuren syndrome in a sibship suggestive of maternal germ-line mosaicism

      AMERICAN JOURNAL OF HUMAN GENETICS
    33. PINGAULT V; BONDURAND N; KUHLBRODT K; GOERICH DE; PREHU MO; PULITI A; HERBARTH B; HERMANSBORGMEYER I; LEGIUS E; MATTHIJS G; AMIEL J; LYONNET S; CECCHERINI I; ROMEO G; SMITH JC; READ AP; WEGNER M; GOOSSENS M
      SOX10 MUTATIONS IN PATIENTS WITH WAARDENBURG-HIRSCHSPRUNG-DISEASE

      Nature genetics
    34. PINGAULT V; BONDURAND N; KUHLBRODT K; GOERICH DE; PREHU MO; PULITI A; LEMORT N; LEGIUS E; MATTHIJS G; AMIEL J; LYONNET S; CECCHERINI I; ROMEO G; CLAYTONSMITH J; READ AP; WEGNER M; GOOSSENS M
      MUTATIONS OF THE SOX10 GENE IN WAARDENBURG-HIRSCHSPRUNG-DISEASE

      European journal of human genetics
    35. SALOMON R; DORAY B; AMIEL J; PELET A; ATTIE T; BACHY B; MUNNICH A; LYONNET S
      RET LIGANDS (GDNF, NEURTURIN) MUTATIONS IN COMBINATION WITH RET MUTATIONS - A MODEL OF MULTIGENIC INHERITANCE IN HIRSCHSPRUNG-DISEASE

      European journal of human genetics
    36. DORAY B; SALOMON R; AMIEL J; PELET A; TOURAINE R; BILLAUD M; ATTIE T; BACHY B; MUNNICH A; LYONNET S
      MUTATION OF THE RET LIGAND, NEURTURIN, SUPPORTS MULTIGENIC INHERITANCE IN HIRSCHSPRUNG-DISEASE

      Human molecular genetics (Print)
    37. DORAY B; SALOMON R; AMIEL J; PELET A; TOURAINE R; BILLAUD M; ATTIE T; BACHY B; MUNNICH A; LYONNET S
      MUTATION OF THE RET LIGAND, NEURTURIN, SUPPORTS MULTIGENIC INHERITANCE IN HIRSCHSPRUNG-DISEASE (VOL 7, PG 1449, 1998)

      Human molecular genetics (Print)
    38. AMIEL J; WATKIN PM; TASSABEHJI M; READ AP; WINTER RM
      MUTATION OF THE MITF GENE IN ALBINISM-DEAFNESS SYNDROME (TIETZ-SYNDROME)

      Clinical dysmorphology
    39. AMIEL J; LACOMBE D; ATTIE T; MUNNICH A; LYONNET S
      FROM CONGENITAL-MALFORMATIONS TO TUMORS I N CHILDREN

      Archives de pediatrie
    40. Salomon, R; Amiel, J; Attie, T; Pelet, A; Munnich, A; Lyonnet, S
      Molecular insights in a multigenic malformation: Hirschsprung disease.

      PATHOLOGIE BIOLOGIE
    41. VABRES P; DELONLAY P; AMIEL J; LYONNET S; MUNNICH A; DEPROST Y
      BLUE-RED AND FUSCO-CERULEUS MACULES - EARLY CUTANEOUS SIGNS OF NEUROFIBROMATOSIS TYPE-I IN CHILDHOOD

      Annales de dermatologie et de venereologie
    42. DELONLAYDEBENEY P; DEBLOIS MC; BONNET D; AMIEL J; ABADIE V; PICQ M; LYONNET S; SIDI D; MUNNICH A; VEKEMANS M; CORMIERDAIRE V
      EBSTEIN ANOMALY ASSOCIATED WITH REARRANGEMENTS OF CHROMOSOMAL REGION 11Q

      American journal of medical genetics
    43. TELLIER AL; CORMIERDAIRE V; ABADIE V; AMIEL J; SIGAUDY S; BONNET D; DELONLAYDEBENEY P; MORRISSEAUDURAND MP; HUBERT P; MICHEL JL; JAN D; DOLLFUS H; BAUMANN C; LABRUNE P; LACOMBE D; PHILIP N; LEMERRER M; BRIARD ML; MUNNICH A; LYONNET S
      CHARGE SYNDROME - REPORT OF 47 CASES AND REVIEW

      American journal of medical genetics
    44. Attie-Bitach, T; Abitbol, M; Gerard, M; Delezoide, AL; Auge, J; Pelet, A; Amiel, J; Pachnis, V; Munnich, A; Lyonnet, S; Vekemans, M
      Expression of the RET proto-oncogene in human embryos

      AMERICAN JOURNAL OF MEDICAL GENETICS
    45. VIOTSZOBOSZLAI G; AMIEL J; DOZ F; PRIEUR M; COUTURIER J; ZUCKER JN; HENRY I; MUNNICH A; VEKEMANS M; LYONNET S
      WILMS-TUMOR AND GONADAL-DYSGENESIS IN A CHILD WITH THE 2Q37.1 DELETION SYNDROME

      Clinical genetics
    46. AMIEL J; SALOMON R; ATTIE T; PELET A; TRANG H; MOKHTARI M; GAULTIER C; MUNNICH A; LYONNET S
      MUTATIONS OF THE RET-GDNF SIGNALING PATHWAY IN ONDINES-CURSE

      American journal of human genetics
    47. BIDAUD C; SALOMON R; VANCAMP G; PELET A; ATTIE T; ENG C; BONDUELLE M; AMIEL J; NIHOULFEKETE C; WILLEMS PJ; MUNNICH A; LYONNET S
      ENDOTHELIN-3 GENE-MUTATIONS IN ISOLATED AND SYNDROMIC HIRSCHSPRUNG-DISEASE

      European journal of human genetics
    48. CHEVALLIER D; BENIZRI E; VOLPE P; AMIEL J; TOUBOL J
      PEYRONIES-DISEASE - REVIEW OF HISTORICAL, EPIDEMIOLOGIC, AND PHYSIOPATHOLOGICAL DATA - DIAGNOSIS AND THERAPEUTIC APPROACH

      La Revue de medecine interne
    49. DELONLAYDEBENEY P; CORMIERDAIRE V; AMIEL J; ABADIE V; ODENT S; PAUPE A; COUDERC S; TELLIER AL; BONNET D; PRIEUR M; VEKEMANS M; MUNNICH A; LYONNET S
      FEATURES OF DIGEORGE-SYNDROME AND CHARGE ASSOCIATION IN 5 PATIENTS

      Journal of Medical Genetics
    50. THAON S; FERRERO C; AUBERGER P; MICHIELS JF; DROZ D; AMIEL J; ROSSI B; POUSTISDELPONT C
      DIFFERENTIAL SP220K EXPRESSION IN RENAL-CARCINOMA AND ONCOCYTOMA CELLS

      International journal of cancer
    51. AMIEL J; ATTIE T; SALOMON R; EDERY P; PELET A; NIHOULFEKETE C; MUNNICH A; LYONNET S
      MOLECULAR-BASIS OF HIRSCHSPRUNGS-DISEASE

      Gut
    52. DELONLAYDEBENEY P; CORMIERDAIRE V; AMIEL J; ABADIE V; BONNET D; PRIEUR M; VEKEMANS M; MUNNICH A; LYONNET S
      DIGEORGE-SYNDROME AND CHARGE ASSOCIATION IN 5 PATIENTS

      American journal of human genetics
    53. AMIEL J; SALOMON R; ATTIE T; MOKHTARI M; TRANG H; GAULTIER C; MUNNICH A; LYONNET S
      IMPAIRED RET SIGNALING PATHWAY IN CONGENITAL CENTRAL HYPOVENTILATION SYNDROME

      American journal of human genetics
    54. DORAY B; SALOMAN R; PELET A; AMIEL J; MUNNICH A; LYONNET S
      EXCLUSION OF ENDOTHELIN-1 AS A CANDIDATE GENE IN MAJOR BRANCHIAL ARCHANOMALY SYNDROMES IN HUMAN

      American journal of human genetics
    55. SALOMON R; ATTIE T; PELET A; BIDAUD C; ENG C; AMIEL J; SARNACKI S; GOULET O; RICOUR C; NIHOULFEKETE C; MUNNICH A; LYONNET S
      GERMLINE MUTATIONS OF THE RET LIGAND GDNF ARE NOT SUFFICIENT TO CAUSEHIRSCHSPRUNG DISEASE

      Nature genetics
    56. EDERY P; ATTIE T; AMIEL J; PELET A; ENG C; HOFSTRA RMW; MARTELLI H; BIDAUD C; MUNNICH A; LYONNET S
      MUTATION OF THE ENDOTHELIN-3 GENE IN THE WAARDENBURG-HIRSCHSPRUNG DISEASE (SHAH-WAARDENBURG SYNDROME)

      Nature genetics
    57. AMIEL J; ATTIE T; JAN D; PELET A; EDERY P; BIDAUD C; LACOMBE D; TAM P; SIMEONI J; FLORI E; NIHOULFEKETE C; MUNNICH A; LYONNET S
      HETEROZYGOUS ENDOTHELIN RECEPTOR-B (EDNRB) MUTATIONS IN ISOLATED HIRSCHSPRUNG DISEASE

      Human molecular genetics
    58. DEMARQUAY JF; CAROLIBOSC FX; HASTIER P; AMIEL J; ZEBOUDJ N; SAINTPAUL MC; DELMONT J
      ISOLATED AND MULTIPLE CYSTIC LIVER METAST ASES OF PROSTATE-CANCER

      Gastroenterologie clinique et biologique
    59. BENIZRI E; FABIANI P; MIGLIORI G; CHEVALLIER D; PEYROTTES A; RAUCOULES M; AMIEL J; MOUIEL J; TOUBOL J
      GANGRENE OF THE PERINEUM

      Urology
    60. BENIZRI EJ; VOLPE P; PUSHKAR D; CHEVALLIER D; AMIEL J; SANIAN H; TOUBOL J
      A NEW VAGINAL PROCEDURE FOR CYSTOCELE REPAIR AND TREATMENT OF STRESS URINARY-INCONTINENCE

      The Journal of urology
    61. BURGLEN L; AMIEL J; VIOLLET L; LEFEBVRE S; BURLET P; CLERMONT O; RACLIN V; LANDRIEU P; VERLOES A; MUNNICH A; MELKI J
      SURVIVAL MOTOR-NEURON GENE DELETION IN THE ARTHROGRYPOSIS MULTIPLEX CONGENITA-SPINAL MUSCULAR-ATROPHY ASSOCIATION

      The Journal of clinical investigation
    62. CARON P; ATTIE T; DAVID D; AMIEL J; BROUSSET F; ROGER P; MUNNICH A; LYONNET S
      C618R MUTATION IN EXON-10 OF THE RET PROTOONCOGENE IN A KINDRED WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A AND HIRSCHSPRUNGS-DISEASE

      The Journal of clinical endocrinology and metabolism
    63. GIOANNI J; ZANGHELLINI E; MAZEAU C; AMIEL J; POUSTISDELPONT C; LAGRANGE JL; DUPLAY H; CALDANI C; COURDI A
      CAL-54, A NEW CELL-LINE DERIVED FROM A HU MAN RENAL-CARCINOMA - CHARACTERIZATION AND RADIOSENSITIVITY

      Bulletin du cancer
    64. ATTIE T; AMIEL J; JAN D; EDERY P; PELET A; SALOMON R; MUNNICH A; LYONNET S; NIHOULFEKETE C
      GENETICS OF HIRSCHSPRUNGS-DISEASE

      Annales de chirurgie
    65. ATTIE T; PELET A; EDERY P; ENG C; MULLIGAN LM; AMIEL J; BOUTRAND L; BELDJORD C; NIHOULFEKETE C; MUNNICH A; PONDER BAJ; LYONNET S
      DIVERSITY OF RET PROTOONCOGENE MUTATIONS IN FAMILIAL AND SPORADIC HIRSCHSPRUNG DISEASE

      Human molecular genetics
    66. ATTIE T; TILL M; PELET A; AMIEL J; EDERY P; BOUTRAND L; MUNNICH A; LYONNET S
      MUTATION OF THE ENDOTHELIN-RECEPTOR-B GENE IN WAARDENBURG-HIRSCHSPRUNG-DISEASE

      Human molecular genetics
    67. ATTIE T; AMIEL J; EDERY P; LYONNET S
      ENDOTHELINS AND ENDOTHELIN RECEPTORS, NEW ACTORS IN DEVELOPMENT

      MS. Medecine sciences
    68. BENIZRI E; VOLPE P; BASTERIS B; POISSON J; CHEVALLIER D; PEYROTTES A; COLOMB F; AMIEL J; KERMAREC J; TOUBOL J
      PREDICTIVE VALUE OF URINE CYTOLOGY IN THE DIAGNOSIS OF UROTHELIAL TUMORS

      Journal d'urologie
    69. AMIEL J; MAZIERE JC; BEUCLER I; KOENIG M; REUTENAUER L; LOUX N; BONNEFONT D; FEO C; LANDRIEU P
      FAMILIAL ISOLATED VITAMIN-E-DEFICIENCY - EXTENSIVE STUDY OF A LARGE FAMILY WITH A 5-YEAR THERAPEUTIC FOLLOW-UP

      Journal of inherited metabolic disease
    70. ATTIE T; TILL M; AMIEL J; EDERY P; PELET A; MUNNICH A; LYONNET S
      ENDOTHELIN RECEPTOR-B GENE MUTATION IN A CONSANGUINEOUS FAMILY WITH WAARDENBURG-HIRSCHSPRUNGS DISEASE

      American journal of human genetics
    71. AMIEL J; ATTIE T; SIMEONI J; EDERY P; GAULTIER C; MUNNICH A; LYONNET S
      MUTATION OF THE RET PROTOONCOGENE IN A PATIENT WITH CONGENITAL CENTRAL HYPOVENTILATION SYNDROME (ONDINES CURSE) AND HIRSCHSPRUNG DISEASE

      American journal of human genetics
    72. AMIEL J; GAGEY V; RABIER D; DORCHE C; BONNEFONT JP; DUFIER JL; SAUDUBRAY JM; REY J; MUNNICH A
      ISOLATED SULFITE OXIDASE DEFICIENCY PRESE NTING AS A LEIGH-SYNDROME

      Archives de pediatrie
    73. FABIANI P; BENIZRI E; IOVINE L; MIGLIORI G; GUGENHEIM J; AMIEL J; TOUBOL J; MOUIEL J
      SURGICAL-TREATMENT OF FOURNIERS GANGRENE

      La Presse medicale
    74. PEYROTTES A; BENIZRI E; CHEVALLIER D; VOLPE P; MICHIELS JF; AMIEL J; TOUBOL J
      RADICAL PROSTATECTOMY AFTER COMPLETE ANDR OGEN BLOCKADE FOR STAGE-B2 AND STAGE-C CANCER OF THE PROSTATE

      Journal d'urologie
    75. BENIZRI E; RAUCOULESAIME M; AMIEL J; TOUBOL J; GRIMAUD D
      COAGULATION DISORDERS AFTER ENDOSCOPIC RE SECTION OF THE PROSTATE

      Journal d'urologie
    76. BENIZRI E; FABIANI P; CASSUTO E; AMIEL J
      LAPAROSCOPIC FENESTRATION OF A POSTTRANSP LANTATION RENAL LYMPHOCELE

      Journal d'urologie
    77. BENIZRI E; WODEY J; AMIEL J; TOUBOL J
      COMPARISON OF 2 PULSED LASERS FOR LITHOTRIPSY OF URETERAL CALCULI - REPORT ON 154 PATIENTS

      The Journal of urology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 29/02/20 alle ore 02:23:21