ACNP - Italian Periodicals Catalogue

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Results: 1-25 | 26-38

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SPORADIC PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY (PHHI) IS A HETEROGENEOUS DISORDER WITH

Authors: VERKARRE V FOURNET JC DELONLAY P RAHIER J ROBERT JJ NIHOULFEKETE C

Citation: V. Verkarre et al., SPORADIC PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY (PHHI) IS A HETEROGENEOUS DISORDER WITH, European journal of human genetics, 6, 1998, pp. 1102-1102

SYNDROME OF CONGENITAL HYPERINSULINISM AND HYPERAMMONEMIA IN 6 UNRELATED PATIENTS

Authors: DELONLAY P FOURNET JC VERKARRE V RAHIER J JUNIEN C NIHOULFEKETE C ROBERT JJ SAUDUBRAY JM

Citation: P. Delonlay et al., SYNDROME OF CONGENITAL HYPERINSULINISM AND HYPERAMMONEMIA IN 6 UNRELATED PATIENTS, European journal of human genetics, 6, 1998, pp. 1105-1105

PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY (PHHI) IS A HETEROGENEOUS DISORDER WITH 2 HISTOLOGICAL FORMS AND DIFFERENT MOLECULAR-BASIS

Authors: DELONLAY P FOURNET JC VERKARRE V RAHIER J ROBERT JJ NIHOULFEKETE C SAUDUBRAY JM JUNIEN C

Citation: P. Delonlay et al., PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY (PHHI) IS A HETEROGENEOUS DISORDER WITH 2 HISTOLOGICAL FORMS AND DIFFERENT MOLECULAR-BASIS, European journal of human genetics, 6, 1998, pp. 1108-1108

PANCREATIC B-CELL PROLIFERATION IN PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY - AN IMMUNOHISTOCHEMICAL STUDY OF 18 CASES

Authors: SEMPOUX C GUIOT Y DUBOIS D NOLLEVAUX MC SAUDUBRAY JM NIHOULFEKETE C RAHIER J

Citation: C. Sempoux et al., PANCREATIC B-CELL PROLIFERATION IN PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY - AN IMMUNOHISTOCHEMICAL STUDY OF 18 CASES, Modern pathology, 11(5), 1998, pp. 444-449

LONG-TERM TREATMENT OF PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY WITH DIAZOXIDE - A RETROSPECTIVE REVIEW OF 77 CASES AND ANALYSISOF EFFICACY-PREDICTING CRITERIA

Authors: TOUATI G POGGITRAVERT F DEBAULNY HO RAHIER J BRUNELLE F NIHOULFEKETE C CZERNICHOW P SAUDUBRAY JM

Citation: G. Touati et al., LONG-TERM TREATMENT OF PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY WITH DIAZOXIDE - A RETROSPECTIVE REVIEW OF 77 CASES AND ANALYSISOF EFFICACY-PREDICTING CRITERIA, European journal of pediatrics, 157(8), 1998, pp. 628-633

PARTIAL OR NEAR-TOTAL PANCREATECTOMY FOR PERSISTENT NEONATAL HYPERINSULINEMIC HYPOGLYCEMIA - THE PATHOLOGISTS ROLE

Authors: RAHIER J SEMPOUX C FOURNET JC POGGI F BRUNELLE F NIHOULFEKETE C SAUDUBRAY JM JAUBERT F

Citation: J. Rahier et al., PARTIAL OR NEAR-TOTAL PANCREATECTOMY FOR PERSISTENT NEONATAL HYPERINSULINEMIC HYPOGLYCEMIA - THE PATHOLOGISTS ROLE, Histopathology, 32(1), 1998, pp. 15-19

UNTITLED - REPLY

Authors: DOMMERGUES M AUBRY MC LORTATJACOB S NIHOULFEKETE C DUMEZ Y

Citation: M. Dommergues et al., UNTITLED - REPLY, Journal of pediatric surgery, 33(5), 1998, pp. 810-810

NEONATAL HYPERINSULINEMIC HYPOGLYCEMIA - HETEROGENEITY OF THE SYNDROME AND KEYS FOR DIFFERENTIAL-DIAGNOSIS

Authors: SEMPOUX C GUIOT Y LEFEVRE A NIHOULFEKETE C JAUBERT F SAUDUBRAY JM RAHIER J

Citation: C. Sempoux et al., NEONATAL HYPERINSULINEMIC HYPOGLYCEMIA - HETEROGENEITY OF THE SYNDROME AND KEYS FOR DIFFERENTIAL-DIAGNOSIS, The Journal of clinical endocrinology and metabolism, 83(5), 1998, pp. 1455-1461

ENDOTHELIN-3 GENE-MUTATIONS IN ISOLATED AND SYNDROMIC HIRSCHSPRUNG-DISEASE

Authors: BIDAUD C SALOMON R VANCAMP G PELET A ATTIE T ENG C BONDUELLE M AMIEL J NIHOULFEKETE C WILLEMS PJ MUNNICH A LYONNET S

Citation: C. Bidaud et al., ENDOTHELIN-3 GENE-MUTATIONS IN ISOLATED AND SYNDROMIC HIRSCHSPRUNG-DISEASE, European journal of human genetics, 5(4), 1997, pp. 247-251

MUTATIONS OF THE EDN3 GENE IN ISOLATED AND SYNDROMIC HIRSCHSPRUNGS-DISEASE

Authors: BIDAUD C SALOMON R EDERY P VANCAMP G PELET A BONDUELLE M NIHOULFEKETE C WILLEMS PJ MUNNICH A LYONNET S

Citation: C. Bidaud et al., MUTATIONS OF THE EDN3 GENE IN ISOLATED AND SYNDROMIC HIRSCHSPRUNGS-DISEASE, Gastroenterologie clinique et biologique, 21(8-9), 1997, pp. 548-554

FAMILIAL ADENOMATOUS POLYPOSIS AND THYROI D-CARCINOMA

Authors: PARAF F OLSCHWANG S NIHOULFEKETE C KAZANDJIAN V BROUSSE N SCHMITZ J

Citation: F. Paraf et al., FAMILIAL ADENOMATOUS POLYPOSIS AND THYROI D-CARCINOMA, Gastroenterologie clinique et biologique, 21(1), 1997, pp. 74-77

A MOSAIC XX XXY IS ASSOCIATED WITH A WIDE SPECTRUM OF INTERSEXUAL STATES/

Authors: SATGE D GENEIX A HASSAN T NIHOULFEKETE C GOBURDHUN J NISHI M MALET P STOLL C

Citation: D. Satge et al., A MOSAIC XX XXY IS ASSOCIATED WITH A WIDE SPECTRUM OF INTERSEXUAL STATES/, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 276-276

SOMATIC DELETION OF THE IMPRINTED 11P15 REGION IN SPORADIC PERSISTENTHYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY IS SPECIFIC OF FOCAL ADENOMATOUS HYPERPLASIA AND ENDORSES PARTIAL PANCREATECTOMY

Authors: DELONLAY P FOURNET JC RAHIER J GROSSMORAND MS POGGITRAVERT F FOUSSIER V BONNEFONT JP BRUSSET MC BRUNELLE F ROBERT JJ NIHOULFEKETE C SAUDUBRAY JM JUNIEN C

Citation: P. Delonlay et al., SOMATIC DELETION OF THE IMPRINTED 11P15 REGION IN SPORADIC PERSISTENTHYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY IS SPECIFIC OF FOCAL ADENOMATOUS HYPERPLASIA AND ENDORSES PARTIAL PANCREATECTOMY, The Journal of clinical investigation, 100(4), 1997, pp. 802-807

MOLECULAR-BASIS OF HIRSCHSPRUNGS-DISEASE

Authors: AMIEL J ATTIE T SALOMON R EDERY P PELET A NIHOULFEKETE C MUNNICH A LYONNET S

Citation: J. Amiel et al., MOLECULAR-BASIS OF HIRSCHSPRUNGS-DISEASE, Gut, 41, 1997, pp. 11-12

SOMATIC DELETION OF THE IMPRINTED 11P15 REGION IN SPORADIC PERSISTENTHYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY IS SPECIFIC OF FOCAL ADENOMATOUS HYPERPLASIA

Authors: DELONLAY P FOURNET JC VERKARRE V RAHIER J GROSSMORAND MS BRUNELLE F ROBERT JJ NIHOULFEKETE C SAUDUBRAY JM JUNIEN C

Citation: P. Delonlay et al., SOMATIC DELETION OF THE IMPRINTED 11P15 REGION IN SPORADIC PERSISTENTHYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY IS SPECIFIC OF FOCAL ADENOMATOUS HYPERPLASIA, American journal of human genetics, 61(4), 1997, pp. 198-198

ANESTHETIC MANAGEMENT FOR ISCHIOPAGUS TETRAPUS CONJOINED TWINS SEPARATION

Authors: CLEMESSY JL BRUSSET MC FROT CM MAYER MN NIHOULFEKETE C BARRIER G

Citation: Jl. Clemessy et al., ANESTHETIC MANAGEMENT FOR ISCHIOPAGUS TETRAPUS CONJOINED TWINS SEPARATION, Paediatric anaesthesia, 6(2), 1996, pp. 160-162

GERMLINE MUTATIONS OF THE RET LIGAND GDNF ARE NOT SUFFICIENT TO CAUSEHIRSCHSPRUNG DISEASE

Authors: SALOMON R ATTIE T PELET A BIDAUD C ENG C AMIEL J SARNACKI S GOULET O RICOUR C NIHOULFEKETE C MUNNICH A LYONNET S

Citation: R. Salomon et al., GERMLINE MUTATIONS OF THE RET LIGAND GDNF ARE NOT SUFFICIENT TO CAUSEHIRSCHSPRUNG DISEASE, Nature genetics, 14(3), 1996, pp. 345-347

HETEROZYGOUS ENDOTHELIN RECEPTOR-B (EDNRB) MUTATIONS IN ISOLATED HIRSCHSPRUNG DISEASE

Authors: 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

Citation: J. Amiel et al., HETEROZYGOUS ENDOTHELIN RECEPTOR-B (EDNRB) MUTATIONS IN ISOLATED HIRSCHSPRUNG DISEASE, Human molecular genetics, 5(3), 1996, pp. 355-357

SERIAL TRANSABDOMINAL AMNIOINFUSION IN THE MANAGEMENT OF GASTROSCHISIS WITH SEVERE OLIGOHYDRAMNIOS

Authors: DOMMERGUES M ANSKER Y AUBRY MC ALEESE JM LORTATJACOB S NIHOULFEKETE C DUMEZ Y

Citation: M. Dommergues et al., SERIAL TRANSABDOMINAL AMNIOINFUSION IN THE MANAGEMENT OF GASTROSCHISIS WITH SEVERE OLIGOHYDRAMNIOS, Journal of pediatric surgery, 31(9), 1996, pp. 1297-1299

GENETICS OF HIRSCHSPRUNGS-DISEASE

Authors: ATTIE T AMIEL J JAN D EDERY P PELET A SALOMON R MUNNICH A LYONNET S NIHOULFEKETE C

Citation: T. Attie et al., GENETICS OF HIRSCHSPRUNGS-DISEASE, Annales de chirurgie, 50(7), 1996, pp. 538-541

TESTICULAR DYSGENESIS DOES NOT AFFECT EXPRESSION OF ANTI-MULLERIAN HORMONE BY SERTOLI CELLS IN PREMEIOTIC SEMINIFEROUS TUBULES

Authors: REY R ALATTAR L LOUIS F JAUBERT F BARBET P NIHOULFEKETE C CHAUSSAIN JL JOSSO N

Citation: R. Rey et al., TESTICULAR DYSGENESIS DOES NOT AFFECT EXPRESSION OF ANTI-MULLERIAN HORMONE BY SERTOLI CELLS IN PREMEIOTIC SEMINIFEROUS TUBULES, The American journal of pathology, 148(5), 1996, pp. 1689-1698

DIVERSITY OF RET PROTOONCOGENE MUTATIONS IN FAMILIAL AND SPORADIC HIRSCHSPRUNG DISEASE

Authors: ATTIE T PELET A EDERY P ENG C MULLIGAN LM AMIEL J BOUTRAND L BELDJORD C NIHOULFEKETE C MUNNICH A PONDER BAJ LYONNET S

Citation: T. Attie et al., DIVERSITY OF RET PROTOONCOGENE MUTATIONS IN FAMILIAL AND SPORADIC HIRSCHSPRUNG DISEASE, Human molecular genetics, 4(8), 1995, pp. 1381-1386

SURGICAL SEPARATION OF CONJOINED (SIAMESE ) OMPHALOPAGUS TWINS AT 2 WEEKS OF AGE

Authors: CAZENEUVE C NIHOULFEKETE C ADAFER M YASSINE B BOURY R WAHHABI M LAJARRIGE C DUMEZ Y AUBRY MC MORIETTE G

Citation: C. Cazeneuve et al., SURGICAL SEPARATION OF CONJOINED (SIAMESE ) OMPHALOPAGUS TWINS AT 2 WEEKS OF AGE, Archives de pediatrie, 2(5), 1995, pp. 452-455

MUTATIONS IN RET PROTOONCOGENE IN HIRSCHS PRUNG DISEASE - A MULTIFUNCTION GENE

Authors: LYONNET S EDERY P ATTIE T NIHOULFEKETE C MUNNICH A

Citation: S. Lyonnet et al., MUTATIONS IN RET PROTOONCOGENE IN HIRSCHS PRUNG DISEASE - A MULTIFUNCTION GENE, MS. Medecine sciences, 10(4), 1994, pp. 450-453

MUTATIONS OF THE RET PROTOONCOGENE IN HIR SCHSPRUNGS-DISEASE

Authors: LYONNET S EDERY P MULLIGAN LM PELET A DOW E ABEL L HOLDER S NIHOULFEKETE C PONDER BAJ MUNNICH A

Citation: S. Lyonnet et al., MUTATIONS OF THE RET PROTOONCOGENE IN HIR SCHSPRUNGS-DISEASE, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 317(4), 1994, pp. 358-362

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