Literature DB >> 1916464

Liver disease in infancy: a 20 year perspective.

G Mieli-Vergani1, E R Howard, A P Mowat.   

Abstract

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Mesh：

Year:  1991        PMID： 1916464      PMCID： PMC1405223          DOI： 10.1136/gut.32.suppl.s123

Source DB:  PubMed          Journal:  Gut        ISSN： 0017-5749            Impact factor:   23.059


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  28 in total

Review 1.  Alpha 1-antitrypsin deficiency, emphysema, and liver disease. Genetic basis and strategies for therapy.

Authors:  R G Crystal
Journal:  J Clin Invest       Date:  1990-05       Impact factor: 14.808

Review 2.  Pathogenesis of alpha 1-antitrypsin deficiency-associated liver disease, 1990.

Authors:  S J Schwarzenberg; H L Sharp
Journal:  J Pediatr Gastroenterol Nutr       Date:  1990-01       Impact factor: 2.839

3.  Prenatal diagnosis of alpha-1-antitrypsin deficiency by fetal blood sampling.

Authors:  G Corney; D B Whitehouse; D A Hopkinson; C H Rodeck; K Nicolaides; M Norman; A P Mowat
Journal:  Prenat Diagn       Date:  1987-02       Impact factor: 3.050

4.  Severe hypertension after liver transplantation in alpha 1 antitrypsin deficiency.

Authors:  G Noble-Jamieson; N D Barnes; S Thiru; A P Mowat
Journal:  Arch Dis Child       Date:  1990-11       Impact factor: 3.791

Review 5.  Genetics of alpha 1-antitrypsin deficiency in relation to neonatal liver disease.

Authors:  S Povey
Journal:  Mol Biol Med       Date:  1990-04

6.  Bacterial cholangitis after surgery for biliary atresia.

Authors:  C Ecoffey; E Rothman; O Bernard; M Hadchouel; J Valayer; D Alagille
Journal:  J Pediatr       Date:  1987-12       Impact factor: 4.406

7.  Syndromic paucity of the intrahepatic bile ducts: diagnostic difficulty; severe morbidity throughout early childhood.

Authors:  A Deprettere; B Portmann; A P Mowat
Journal:  J Pediatr Gastroenterol Nutr       Date:  1987 Nov-Dec       Impact factor: 2.839

8.  Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases.

Authors:  D Alagille; A Estrada; M Hadchouel; M Gautier; M Odièvre; J P Dommergues
Journal:  J Pediatr       Date:  1987-02       Impact factor: 4.406

9.  HLA phenotypes and gene polymorphisms in juvenile liver disease associated with alpha 1-antitrypsin deficiency.

Authors:  D G Doherty; P T Donaldson; D B Whitehouse; G Mieli-Vergani; A Duthie; D A Hopkinson; A P Mowat
Journal:  Hepatology       Date:  1990-08       Impact factor: 17.425

10.  Results of surgical treatment for extrahepatic biliary atresia in United Kingdom 1980-2. Survey conducted on behalf of the British Paediatric Association Gastroenterology Group and the British Association of Paediatric Surgeons.

Authors:  J W McClement; E R Howard; A P Mowat
Journal:  Br Med J (Clin Res Ed)       Date:  1985-02-02
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  13 in total

1.  Early Diagnosis of ABCB11 Spectrum Liver Disorders by Next Generation Sequencing.

Authors:  Su Jeong Lee; Jung Eun Kim; Byung-Ho Choe; An Na Seo; Han-Ik Bae; Su-Kyeong Hwang
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2017-06-28

2.  Niemann-Pick disease type C in the newborn period: a single-center experience.

Authors:  Ersin Gumus; Goknur Haliloglu; Asuman Nur Karhan; Hulya Demir; Figen Gurakan; Meral Topcu; Aysel Yuce
Journal:  Eur J Pediatr       Date:  2017-09-27       Impact factor: 3.183

3.  The usefulness of bone marrow aspiration in the diagnosis of Niemann-Pick disease type C in infantile liver disease.

Authors:  A F Rodrigues; R G Gray; M A Preece; R Brown; F G Hill; U Baumann; P J McKiernan
Journal:  Arch Dis Child       Date:  2006-05-31       Impact factor: 3.791

4.  Significance of low or normal serum gamma glutamyl transferase level in infants with idiopathic neonatal hepatitis.

Authors:  Jian She Wang; Nancy Tan; Anil Dhawan
Journal:  Eur J Pediatr       Date:  2006-06-13       Impact factor: 3.183

5.  Genetic variation in the mouse model of Niemann Pick C1 affects female, as well as male, adiposity, and hepatic bile transporters but has indeterminate effects on caveolae.

Authors:  David A Jelinek; Bita Maghsoodi; Ivan A Borbon; Rhiannon N Hardwick; Nathan J Cherrington; Robert P Erickson
Journal:  Gene       Date:  2011-10-14       Impact factor: 3.688

6.  The natural history of Niemann-Pick disease type C in the UK.

Authors:  J Imrie; S Dasgupta; G T N Besley; C Harris; L Heptinstall; S Knight; M T Vanier; A H Fensom; C Ward; E Jacklin; C Whitehouse; J E Wraith
Journal:  J Inherit Metab Dis       Date:  2006-12-11       Impact factor: 4.982

7.  Analysis of the histologic features in the differential diagnosis of intrahepatic neonatal cholestasis.

Authors:  Maria Angela Bellomo-Brandao; Cecilia A F Escanhoela; Luciana R Meirelles; Gilda Porta; Gabriel Hessel
Journal:  World J Gastroenterol       Date:  2009-01-28       Impact factor: 5.742

8.  The role of decreased levels of Niemann-Pick C1 intracellular cholesterol transport on obesity is reversed in the C57BL/6J, metabolic syndrome mouse strain: a metabolic or an inflammatory effect?

Authors:  Ivan Borbon; Erin Campbell; Wangjing Ke; Robert P Erickson
Journal:  J Appl Genet       Date:  2012-05-15       Impact factor: 3.240

9.  Hepatocellular carcinoma as a complication of Niemann-Pick disease type C1.

Authors:  Jorge L Rodriguez-Gil; Simona E Bianconi; Nicole Farhat; David E Kleiner; Marie Nelson; Forbes D Porter
Journal:  Am J Med Genet A       Date:  2021-06-17       Impact factor: 2.578

10.  Diversity of disorders causing neonatal cholestasis - the experience of a tertiary pediatric center in Germany.

Authors:  André Hoerning; Simon Raub; Alexander Dechêne; Michelle N Brosch; Simone Kathemann; Peter F Hoyer; Patrick Gerner
Journal:  Front Pediatr       Date:  2014-06-23       Impact factor: 3.418
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