AAAAAA

   
Results: 1-25 | 26-37
Results: 1-25/37
THE ALAGILLES-SYNDROME AND ITS ANESTHETIC CONSIDERATIONS
Authors: CHOUDHRY DK REHMAN MA SCHWARTZ RE PICCOLI DA
Citation: Dk. Choudhry et al., THE ALAGILLES-SYNDROME AND ITS ANESTHETIC CONSIDERATIONS, Paediatric anaesthesia, 8(1), 1998, pp. 79-82
RUPTURED RETROCECAL APPENDICITIS IN AN ADOLESCENT PRESENTING AS PORTAL-MESENTERIC THROMBOSIS AND PYLEPHLEBITIS
Authors: KADER HA BALDASSANO RN HARTY MP NICOTRA JJ VONALLMEN D FINN L MARKOWITZ J CARRIER M PICCOLI DA
Citation: Ha. Kader et al., RUPTURED RETROCECAL APPENDICITIS IN AN ADOLESCENT PRESENTING AS PORTAL-MESENTERIC THROMBOSIS AND PYLEPHLEBITIS, Journal of pediatric gastroenterology and nutrition, 27(5), 1998, pp. 584-588
RECURRENT PERICARDITIS DUE TO MESALAMINE HYPERSENSITIVITY - A PEDIATRIC CASE-REPORT AND REVIEW OF THE LITERATURE
Authors: SENTONGO TAS PICCOLI DA
Citation: Tas. Sentongo et Da. Piccoli, RECURRENT PERICARDITIS DUE TO MESALAMINE HYPERSENSITIVITY - A PEDIATRIC CASE-REPORT AND REVIEW OF THE LITERATURE, Journal of pediatric gastroenterology and nutrition, 27(3), 1998, pp. 344-347
JAGGED1 EXPRESSION IN THE DEVELOPING LIVER - CORRELATION WITH HISTOLOGIC FEATURES IN ALAGILLE-SYNDROME
Authors: LOOMES KM SPINNER NB PICCOLI DA OAKEY RJ PHIL D
Citation: Km. Loomes et al., JAGGED1 EXPRESSION IN THE DEVELOPING LIVER - CORRELATION WITH HISTOLOGIC FEATURES IN ALAGILLE-SYNDROME, Hepatology, 28(4), 1998, pp. 618-618
CHRONIC INTESTINAL PSEUDOOBSTRUCTION AS A PRESENTING FEATURE IN MITOCHONDRIAL ENCEPHALOMYOPATHIES
Authors: VERMA A BERRY GT PICCOLI DA MORAES CT
Citation: A. Verma et al., CHRONIC INTESTINAL PSEUDOOBSTRUCTION AS A PRESENTING FEATURE IN MITOCHONDRIAL ENCEPHALOMYOPATHIES, Neurology, 50(4), 1998, pp. 3003-3003
CLOSTRIDIUM-DIFFICILE TOXIN-A AND TOXIN-B IN SYMPTOMATIC PATIENTS AT A TERTIARY PEDIATRIC HOSPITAL
Authors: KADER HA PICCOLI DA JAWAD AF MCGOWAN KL MALLER ES
Citation: Ha. Kader et al., CLOSTRIDIUM-DIFFICILE TOXIN-A AND TOXIN-B IN SYMPTOMATIC PATIENTS AT A TERTIARY PEDIATRIC HOSPITAL, Gastroenterology, 114(4), 1998, pp. 85-85
A STUDY OF PANCREATIC FUNCTION IN 17 CHILDREN WITH ALAGILLE-SYNDROME
Authors: JOHN HA LOOMES K WEYLER R STALLINGS V PICCOLI DA MULBERG AE
Citation: Ha. John et al., A STUDY OF PANCREATIC FUNCTION IN 17 CHILDREN WITH ALAGILLE-SYNDROME, Gastroenterology, 114(4), 1998, pp. 3630-3630
MOLECULAR ANALYSIS OF JAGGEDI IN 26 ALAGILLE SYNDROME FAMILIES DEMONSTRATES THAT NEARLY ALL MUTATIONS ARE PRIVATE AND RESULT IN PREMATURE PROTEIN TERMINATION AND LOSS OF THE TRANSMEMBRANE DOMAIN
Authors: KRANTZ I SPINNER NB COLLITON R GENIN A PICCOLI DA
Citation: I. Krantz et al., MOLECULAR ANALYSIS OF JAGGEDI IN 26 ALAGILLE SYNDROME FAMILIES DEMONSTRATES THAT NEARLY ALL MUTATIONS ARE PRIVATE AND RESULT IN PREMATURE PROTEIN TERMINATION AND LOSS OF THE TRANSMEMBRANE DOMAIN, Gastroenterology, 114(4), 1998, pp. 3649-3649
NEONATAL RENAL-INSUFFICIENCY AND RENAL ACIDOSIS ARE MANIFESTATIONS OFALAGILLE SYNDROME IN INFANCY
Authors: MCBRIDE KE PICCOLI DA
Citation: Ke. Mcbride et Da. Piccoli, NEONATAL RENAL-INSUFFICIENCY AND RENAL ACIDOSIS ARE MANIFESTATIONS OFALAGILLE SYNDROME IN INFANCY, Gastroenterology, 114(4), 1998, pp. 3664-3664
SPECTRUM AND FREQUENCY OF JAGGED1 (JAG1) MUTATIONS IN ALAGILLE-SYNDROME PATIENTS AND THEIR FAMILIES
Authors: KRANTZ ID COLLITON RP GENIN A RAND EB LI LH PICCOLI DA SPINNER NB
Citation: Id. Krantz et al., SPECTRUM AND FREQUENCY OF JAGGED1 (JAG1) MUTATIONS IN ALAGILLE-SYNDROME PATIENTS AND THEIR FAMILIES, American journal of human genetics, 62(6), 1998, pp. 1361-1369
MUTATIONS IN THE HUMAN JAGGED1 GENE ARE RESPONSIBLE FOR ALAGILLE-SYNDROME
Authors: ODA T ELKAHLOUN AG PIKE BL OKAJIMA K KRANTZ ID GENIN A PICCOLI DA MELTZER PS SPINNER NB COLLINS FS CHANDRASEKHARAPPA SC
Citation: T. Oda et al., MUTATIONS IN THE HUMAN JAGGED1 GENE ARE RESPONSIBLE FOR ALAGILLE-SYNDROME, Nature genetics, 16(3), 1997, pp. 235-242
ALAGILLE-SYNDROME IS CAUSED BY MUTATIONS IN HUMAN JAGGED1, WHICH ENCODES A LIGAND FOR NOTCH1
Authors: LI LH KRANTZ ID DENG Y GENIN A BANTA AB COLLINS CC QI M TRASK BJ KUO WL COCHRAN J COSTA T PIERPONT MEM RAND EB PICCOLI DA HOOD L SPINNER NB
Citation: Lh. Li et al., ALAGILLE-SYNDROME IS CAUSED BY MUTATIONS IN HUMAN JAGGED1, WHICH ENCODES A LIGAND FOR NOTCH1, Nature genetics, 16(3), 1997, pp. 243-251
INFLUENCE OF BONE-AGE ON BONE-MINERAL DENSITY ASSESSMENT IN CHILDREN WITH CROHNS-DISEASE
Authors: SEMEAO EJ JAWAD AF ZEMEL BS PICCOLI DA STALLINGS VA
Citation: Ej. Semeao et al., INFLUENCE OF BONE-AGE ON BONE-MINERAL DENSITY ASSESSMENT IN CHILDREN WITH CROHNS-DISEASE, Journal of bone and mineral research, 12, 1997, pp. 595-595
GENETIC AND MORPHOLOGICAL FINDINGS IN PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS (BYLER-DISEASE [PFIC-1] AND BYLER-SYNDROME) - EVIDENCE FOR HETEROGENEITY
Authors: BULL LN CARLTON VEH STRICKER NL BAHARLOO S DEYOUNG JA FREIMER NB MAGID MS KAHN E MARKOWITZ J DICARLO FJ MCLOUGHLIN L BOYLE JT DAHMS BB FAUGHT PR FITZGERALD JF PICCOLI DA WITZLEBEN CL OCONNELL NC SETCHELL KDR AGOSTINI RM KOCOSHIS SA REYES J KNISELY AS
Citation: Ln. Bull et al., GENETIC AND MORPHOLOGICAL FINDINGS IN PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS (BYLER-DISEASE [PFIC-1] AND BYLER-SYNDROME) - EVIDENCE FOR HETEROGENEITY, Hepatology, 26(1), 1997, pp. 155-164
COLITIS ASSOCIATED WITH ALPHA-INTERFERON
Authors: WENNER WJ PICCOLI DA
Citation: Wj. Wenner et Da. Piccoli, COLITIS ASSOCIATED WITH ALPHA-INTERFERON, Journal of clinical gastroenterology, 25(1), 1997, pp. 398-399
CHRONIC INTESTINAL PSEUDOOBSTRUCTION ASSOCIATED WITH FETAL ALCOHOL SYNDROME
Authors: UC A VASILIAUSKAS E PICCOLI DA FLORES AF DILORENZO C HYMAN PE
Citation: A. Uc et al., CHRONIC INTESTINAL PSEUDOOBSTRUCTION ASSOCIATED WITH FETAL ALCOHOL SYNDROME, Digestive diseases and sciences, 42(6), 1997, pp. 1163-1167
DELETIONS OF 20P12 IN ALAGILLE-SYNDROME - FREQUENCY AND MOLECULAR CHARACTERIZATION
Authors: KRANTZ ID RAND EB GENIN A HUNT P JONES M LOUIS AA GRAHAM JM BHATT S PICCOLI DA SPINNER NB
Citation: Id. Krantz et al., DELETIONS OF 20P12 IN ALAGILLE-SYNDROME - FREQUENCY AND MOLECULAR CHARACTERIZATION, American journal of medical genetics, 70(1), 1997, pp. 80-86
A NOVEL MITOCHONDRIAL G8313A MUTATION ASSOCIATED WITH PROMINENT INITIAL GASTROINTESTINAL SYMPTOMS AND PROGRESSIVE ENCEPHALONEUROPATHY
Authors: VERMA A PICCOLI DA BONILLA E BERRY GT DIMAURO S MORAES CT
Citation: A. Verma et al., A NOVEL MITOCHONDRIAL G8313A MUTATION ASSOCIATED WITH PROMINENT INITIAL GASTROINTESTINAL SYMPTOMS AND PROGRESSIVE ENCEPHALONEUROPATHY, Pediatric research, 42(4), 1997, pp. 448-454
ALAGILLE SYNDROME
Authors: KRANTZ ID PICCOLI DA SPINNER NB
Citation: Id. Krantz et al., ALAGILLE SYNDROME, Journal of Medical Genetics, 34(2), 1997, pp. 152-157
VERTEBRAL COMPRESSION FRACTURES IN PEDIATRIC-PATIENTS WITH CROHNS-DISEASE
Authors: SEMEAO EJ STALLINGS VA PECK SN PICCOLI DA
Citation: Ej. Semeao et al., VERTEBRAL COMPRESSION FRACTURES IN PEDIATRIC-PATIENTS WITH CROHNS-DISEASE, Gastroenterology, 112(5), 1997, pp. 1710-1713
AN ANALYSIS OF PANCREATIC AND NUTRITIONAL-STATUS IN CHILDREN WITH ALAGILLE-SYNDROME
Authors: JOHN HA WASSERMAN D STALLINGS V PICCOLI DA MULBERG AE
Citation: Ha. John et al., AN ANALYSIS OF PANCREATIC AND NUTRITIONAL-STATUS IN CHILDREN WITH ALAGILLE-SYNDROME, Gastroenterology, 112(4), 1997, pp. 883-883
CROHNS-DISEASE (CD) AND ULCERATIVE-COLITIS (UC) IN A PEDIATRIC POPULATION - CHARACTERISTICS, ETHNICITY AND RELATIVE FREQUENCY
Authors: JESHION WC BALDASSANO RN HAN PD PICCOLI DA
Citation: Wc. Jeshion et al., CROHNS-DISEASE (CD) AND ULCERATIVE-COLITIS (UC) IN A PEDIATRIC POPULATION - CHARACTERISTICS, ETHNICITY AND RELATIVE FREQUENCY, Gastroenterology, 112(4), 1997, pp. 1006-1006
MUTATIONS IN JAGGED1 (JAG1) CAUSE ALAGILLE-SYNDROME
Authors: KRANTZ ID LI L COLLITON RP GENIN A RAND E PICCOLI DA HOOD L SPINNER NB
Citation: Id. Krantz et al., MUTATIONS IN JAGGED1 (JAG1) CAUSE ALAGILLE-SYNDROME, American journal of human genetics, 61(4), 1997, pp. 43-43
HUMAN JAGGED-1 (JAG1) - FUNCTIONS IN REGULATION OF MYELOID PROGENITOR-CELL DIFFERENTIATION AND ROLES IN ETIOLOGY OF DEVELOPMENTAL ABNORMALITIES SUCH AS SEEN IN ALAGILLE-SYNDROME
Authors: LI L KRANTZ ID DENG Y GENIN A BANTA AB QI M TOROKSTORB B MILNER L TRASK BJ PICCOLI DA SPINNER NB HOOD L
Citation: L. Li et al., HUMAN JAGGED-1 (JAG1) - FUNCTIONS IN REGULATION OF MYELOID PROGENITOR-CELL DIFFERENTIATION AND ROLES IN ETIOLOGY OF DEVELOPMENTAL ABNORMALITIES SUCH AS SEEN IN ALAGILLE-SYNDROME, American journal of human genetics, 61(4), 1997, pp. 1980-1980
A NOVEL MITOCHONDRIAL-DNA G8313A MUTATION ASSOCIATED WITH SEVERE CHILDHOOD ENCEPHALOMYOPATHY
Authors: VERMA A MORAES CT PICCOLI DA BERRY GT
Citation: A. Verma et al., A NOVEL MITOCHONDRIAL-DNA G8313A MUTATION ASSOCIATED WITH SEVERE CHILDHOOD ENCEPHALOMYOPATHY, Annals of neurology, 40(3), 1996, pp. 204-204
Risultati: 1-25 | 26-37