Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Familial intrahepatic cholestatic jaundice in infancy.

Literature DB >> 5940621

Familial intrahepatic cholestatic jaundice in infancy.

O P Gray, R A Saunders.

Abstract

Entities: Disease

Mesh：

Substances：

Year: 1966 PMID： 5940621 PMCID： PMC2019567 DOI： 10.1136/adc.41.217.320

Source DB: PubMed Journal: Arch Dis Child ISSN： 0003-9888 Impact factor: 3.791

× No keyword cloud information.

10 in total

1. IDIOPATHIC RECURRENT CHOLESTASIS: A STUDY OF THE FUNCTIONAL AND PATHOLOGICAL LESIONS IN FOUR CASES.

Authors: R WILLIAMS; M A CARTTER; S SHERLOCK; P J SCHEUER; K R HILL
Journal: Q J Med Date: 1964-07

2. Studies of chronic familial non-hemolytic jaundice with conjugated bilirubin in the serum with and without an unidentified pigment in the liver cells.

Authors: I M ARIAS
Journal: Am J Med Date: 1961-10 Impact factor: 4.965

3. Benign recurrent intrahepatic cholestasis.

Authors: R H SCHAPIRO; K J ISSELBACHER
Journal: N Engl J Med Date: 1963-03-28 Impact factor: 91.245

4. Familial nonhemolytic jaundice with conjugated bilirubin in the serum; a case study.

Authors: L SCHIFF; B H BILLING; Y OIKAWA
Journal: N Engl J Med Date: 1959-06-25 Impact factor: 91.245

5. The serum trihydroxy-dihydroxy bile acid ratio in liver and biliary tract disease.

Authors: J B CAREY
Journal: J Clin Invest Date: 1958-11 Impact factor: 14.808

6. Congenital absence of the intrahepatic bile ducts.

Authors: L HAAS; R H DOBBS
Journal: Arch Dis Child Date: 1958-10 Impact factor: 3.791

7. Morphologic studies of cholestasis.

Authors: F SCHAFFNER; H POPPER
Journal: Gastroenterology Date: 1959-11 Impact factor: 22.682

8. Congenital familial nonhemolytic jaundice with kernicterus.

Authors: J F CRIGLER; V A NAJJAR
Journal: Pediatrics Date: 1952-08 Impact factor: 7.124

9. Chronic idiopathic jaundice with unidentified pigment in liver cells; a new clinicopathologic entity with a report of 12 cases.

Authors: I N DUBIN; F B JOHNSON
Journal: Medicine (Baltimore) Date: 1954-09 Impact factor: 1.889

10. Studies on the Fine Structure of the Terminal Branches of the Biliary Tree: II. Observations of Pathologically Altered Bile Canaliculi.

Authors: J W Steiner; J S Carruthers
Journal: Am J Pathol Date: 1961-07 Impact factor: 4.307

10 in total

1. Progressive intrahepatic cholestasis (Byler's disease): case report.

Authors: R De Vos; C de Wolf-Peeters; V Desmet; E Eggermont; K Van Acker
Journal: Gut Date: 1975-12 Impact factor: 23.059

Review 2. Liver transplantation and the management of progressive familial intrahepatic cholestasis in children.

Authors: Ashley Mehl; Humberto Bohorquez; Maria-Stella Serrano; Gretchen Galliano; Trevor W Reichman
Journal: World J Transplant Date: 2016-06-24

3. Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.

Authors: C Bétard; A Rasquin-Weber; C Brewer; E Drouin; S Clark; A Verner; C Darmond-Zwaig; J Fortin; J Mercier; P Chagnon; T M Fujiwara; K Morgan; A Richter; T J Hudson; G A Mitchell
Journal: Am J Hum Genet Date: 2000-05-11 Impact factor: 11.025

9. [Hypertension and bilateral stenosis of the renal artery associated with congenital hypoplasia of the intrahepatic bile ducts (author's transl)].

Authors: R Exss; H W Rotthauwe
Journal: Eur J Pediatr Date: 1976-01-02 Impact factor: 3.183

10. Pathology of chronic vitamin E deficiency in fatal familial intrahepatic cholestasis (Byler disease).

Authors: K Saito; S Matsumoto; T Yokoyama; M Okaniwa; S Kamoshita
Journal: Virchows Arch A Pathol Anat Histol Date: 1982-08

10 in total

Familial intrahepatic cholestatic jaundice in infancy.

1. IDIOPATHIC RECURRENT CHOLESTASIS: A STUDY OF THE FUNCTIONAL AND PATHOLOGICAL LESIONS IN FOUR CASES.

2. Studies of chronic familial non-hemolytic jaundice with conjugated bilirubin in the serum with and without an unidentified pigment in the liver cells.

3. Benign recurrent intrahepatic cholestasis.

4. Familial nonhemolytic jaundice with conjugated bilirubin in the serum; a case study.

5. The serum trihydroxy-dihydroxy bile acid ratio in liver and biliary tract disease.

6. Congenital absence of the intrahepatic bile ducts.

7. Morphologic studies of cholestasis.

8. Congenital familial nonhemolytic jaundice with kernicterus.

9. Chronic idiopathic jaundice with unidentified pigment in liver cells; a new clinicopathologic entity with a report of 12 cases.

10. Studies on the Fine Structure of the Terminal Branches of the Biliary Tree: II. Observations of Pathologically Altered Bile Canaliculi.

1. Progressive intrahepatic cholestasis (Byler's disease): case report.

Review 2. Liver transplantation and the management of progressive familial intrahepatic cholestasis in children.

3. Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.

4. Severe familial intrahepatic cholestasis.

5. [Benign recurrent intrahepatic cholestasis].

6. Hereditary recurrent intrahepatic cholestasis from birth.

7. Fatal familial cholestatic syndrome in Greenland Eskimo children. A histomorphological analysis of 16 cases.

8. Byler-like familial cholestasis in an extended kindred.

9. [Hypertension and bilateral stenosis of the renal artery associated with congenital hypoplasia of the intrahepatic bile ducts (author's transl)].

10. Pathology of chronic vitamin E deficiency in fatal familial intrahepatic cholestasis (Byler disease).