ACNP - Italian Periodicals Catalogue

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Results: 1-16 |

Results: 16

ASSOCIATION OF MULTIPLE ENDOCRINE NEOPLASIA TYPE-2 AND HIRSCHSPRUNG-DISEASE

Authors: ROMEO G CECCHERINI I CELLI J PRIOLO M BETSOS N BONARDI G SERI M YIN L LERONE M JASONNI V MARTUCCIELLO G

Citation: G. Romeo et al., ASSOCIATION OF MULTIPLE ENDOCRINE NEOPLASIA TYPE-2 AND HIRSCHSPRUNG-DISEASE, Journal of internal medicine, 243(6), 1998, pp. 515-520

UPDATE ON BASIC RESEARCH ON HIRSCHSPRUNGS-DISEASE

Authors: MARTUCCIELLO G HOLSCHNEIDER AM

Citation: G. Martucciello et Am. Holschneider, UPDATE ON BASIC RESEARCH ON HIRSCHSPRUNGS-DISEASE, European journal of pediatric surgery, 8(3), 1998, pp. 131-132

GDNF DEFICIT IN HIRSCHSPRUNGS-DISEASE

Authors: MARTUCCIELLO G THOMPSON H MAZZOLA C MORANDO A BERTAGNON M NEGRI F BRIZZOLARA A ROCCHETTI L GAMBINI C JASONNI V

Citation: G. Martucciello et al., GDNF DEFICIT IN HIRSCHSPRUNGS-DISEASE, Journal of pediatric surgery, 33(1), 1998, pp. 99-102

FREQUENCY OF RET MUTATIONS IN LONG-SEGMENT AND SHORT-SEGMENT HIRSCHSPRUNG DISEASE

Authors: SERI M YIN L BARONE V BOLINO A CELLI I BOCCIARDI R PASINI B CECCHERINI I LERONE M KRISTOFFERSSON U LARSSON LT CASASA JM CASS DT ABRAMOWICZ MJ VANDERWINDEN JM KRAVCENKIENE I BARIC I SILENGO M MARTUCCIELLO G ROMEO G

Citation: M. Seri et al., FREQUENCY OF RET MUTATIONS IN LONG-SEGMENT AND SHORT-SEGMENT HIRSCHSPRUNG DISEASE, Human mutation, 9(3), 1997, pp. 243-249

INTESTINAL MICROVILLOUS ATROPHY AND TRANSIENT NEURONAL DYSPLASIA

Authors: ROGGERO P MAZZOLA C FAVA G BAGOZZI DC MARTUCCIELLO G LUZZANI S

Citation: P. Roggero et al., INTESTINAL MICROVILLOUS ATROPHY AND TRANSIENT NEURONAL DYSPLASIA, Transplantation proceedings, 29(3), 1997, pp. 1868-1869

HIRSCHSPRUNGS-DISEASE AS A NEUROCHRISTOPATHY

Authors: MARTUCCIELLO G

Citation: G. Martucciello, HIRSCHSPRUNGS-DISEASE AS A NEUROCHRISTOPATHY, Pediatric surgery international, 12(1), 1996, pp. 2-10

RET PROTEIN IN THE HUMAN FETAL RECTUM

Authors: TAM PKH GOULD SJ MARTUCCIELLO G BIDDOLPH S TAKAHASHI M JASONNI V

Citation: Pkh. Tam et al., RET PROTEIN IN THE HUMAN FETAL RECTUM, Journal of pediatric surgery, 31(4), 1996, pp. 568-571

IMMUNOHISTOCHEMICAL LOCALIZATION OF RET PROTEIN IN HIRSCHSPRUNGS-DISEASE

Authors: MARTUCCIELLO G FAVRE A TAKAHASHI M JASONNI V

Citation: G. Martucciello et al., IMMUNOHISTOCHEMICAL LOCALIZATION OF RET PROTEIN IN HIRSCHSPRUNGS-DISEASE, Journal of pediatric surgery, 30(3), 1995, pp. 433-436

NEURONAL INTESTINAL DYSPLASIA - CLINICAL-EXPERIENCE IN ITALIAN PATIENTS

Authors: MARTUCCIELLO G CAFFARENA PE LERONE M MATTIOLI G BARABINO A BISIO G JASONNI W

Citation: G. Martucciello et al., NEURONAL INTESTINAL DYSPLASIA - CLINICAL-EXPERIENCE IN ITALIAN PATIENTS, European journal of pediatric surgery, 4(5), 1994, pp. 287-292

LONG-GAP ESOPHAGEAL ATRESIA - A COMBINED ENDOSCOPIC AND RADIOLOGIC EVALUATION

Authors: CAFFARENA PE MATTIOLI G BISIO G MARTUCCIELLO G IVANI G JASONNI V

Citation: Pe. Caffarena et al., LONG-GAP ESOPHAGEAL ATRESIA - A COMBINED ENDOSCOPIC AND RADIOLOGIC EVALUATION, European journal of pediatric surgery, 4(2), 1994, pp. 67-69

THE GENETICS OF HIRSCHSPRUNG DISEASE AND THE CONCEPT OF PHENOTYPIC DIVERSITY DUE TO ALLELIC SERIES

Authors: ROMEO G LERONE M PASINI B YIN L CECCHERINI I BARONE V BOLINO A SERI M MARTUCCIELLO G

Citation: G. Romeo et al., THE GENETICS OF HIRSCHSPRUNG DISEASE AND THE CONCEPT OF PHENOTYPIC DIVERSITY DUE TO ALLELIC SERIES, Rivista italiana di pediatria, 20(4), 1994, pp. 441-445

POINT MUTATIONS AFFECTING THE TYROSINE KINASE DOMAIN OF THE RET PROTOONCOGENE IN HIRSCHPRUNGS DISEASE

Authors: ROMEO G RONCHETTO P LUO Y BARONE V SERI M CECCHERINI I PASINI B BOCCIARDI R LERONE M KAARIAINEN H MARTUCCIELLO G

Citation: G. Romeo et al., POINT MUTATIONS AFFECTING THE TYROSINE KINASE DOMAIN OF THE RET PROTOONCOGENE IN HIRSCHPRUNGS DISEASE, Nature, 367(6461), 1994, pp. 377-378

A GENE FOR HIRSCHSPRUNG DISEASE MAPS TO THE PROXIMAL LONG ARM OF CHROMOSOME-10

Authors: LYONNET S BOLINO A PELET A ABEL L NIHOULFEKETE C BRIARD ML MOKSIU V KAARIAINEN H MARTUCCIELLO G LERONE M PULITI A LUO Y WEISSENBACH J DEVOTO M MUNNICH A ROMEO G

Citation: S. Lyonnet et al., A GENE FOR HIRSCHSPRUNG DISEASE MAPS TO THE PROXIMAL LONG ARM OF CHROMOSOME-10, Nature genetics, 4(4), 1993, pp. 346-350

USE OF STAPLERS IN CONGENITAL LOBAR EMPHYSEMA

Authors: MATTIOLI G CAGNAZZO A MARTUCCIELLO G JASOUNI V

Citation: G. Mattioli et al., USE OF STAPLERS IN CONGENITAL LOBAR EMPHYSEMA, European journal of pediatric surgery, 3(6), 1993, pp. 359-361

DELETED AND NORMAL CHROMOSOME 10 HOMOLOGS FROM A PATIENT WITH HIRSCHSPRUNG DISEASE ISOLATED IN 2 CELL HYBRIDS THROUGH ENRICHMENT BY IMMUNOMAGNETIC SELECTION

Authors: PULITI A COVONE AE BICOCCHI MP BOLINO A LERONE M MARTUCCIELLO G JASONNI V ROMEO G

Citation: A. Puliti et al., DELETED AND NORMAL CHROMOSOME 10 HOMOLOGS FROM A PATIENT WITH HIRSCHSPRUNG DISEASE ISOLATED IN 2 CELL HYBRIDS THROUGH ENRICHMENT BY IMMUNOMAGNETIC SELECTION, Cytogenetics and cell genetics, 63(2), 1993, pp. 102-106

UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, AND BRACHYDACTYLY - REPORT OF A NEW PATIENT WITH ADDITIONAL FINDINGS

Authors: SILENGO M LERONE M ROMEO G CALCAGNO E MARTUCCIELLO G JASONNI V

Citation: M. Silengo et al., UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, AND BRACHYDACTYLY - REPORT OF A NEW PATIENT WITH ADDITIONAL FINDINGS, American journal of medical genetics, 47(6), 1993, pp. 931-933

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