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Pediatrics, ISSN 0031-4005, 08/2016, Volume 138, Issue 2, p. e1
  Cholestatic liver disease has long been associated with childhood rickets, secondary to impaired absorption of fat-soluble vitamin D. Elevated serum levels... 
Babies | Liver diseases | Genetic disorders | Vitamin D | Metabolism
Journal Article
Hepatology (Baltimore, Md.), ISSN 0270-9139, 4/2018, Volume 67, Issue 4, pp. 1531 - 1545
Bile salt export pump BSEP (ABCB11) is a liver-specific adenosine triphosphate-cassette binding transporter that mediates canalicular bile salt excretion from... 
canalicular transporter | Mdr1 | PFIC2 | BSEP | rapamycin
Journal Article
Journal of Pediatric Gastroenterology and Nutrition, ISSN 0277-2116, 02/2018, Volume 66, Issue 2, pp. e57 - e59
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 03/2017, Volume 41, Issue 3, pp. 354 - 364
Cystic biliary atresia (CBA), a rare cystic expansion of atretic extrahepatic bile ducts in young infants, overlaps in age at presentation and imaging features... 
biliary atresia | cystic biliary malformation | biliary cyst | choledochal cyst | cystic biliary atresia | SURGERY | ETIOLOGY | BILE-DUCT | PATHOLOGY | SUBGROUP | Biliary Atresia - diagnosis | Choledochal Cyst - diagnosis | Diagnosis, Differential | Humans | Female | Infant | Male | Bile Ducts, Extrahepatic - pathology | Biliary Atresia - pathology | Infant, Newborn | Choledochal Cyst - pathology
Journal Article
Journal Article
Journal Article
Digestive Diseases and Sciences, ISSN 0163-2116, 09/2019
Journal Article
Gastroenterology, ISSN 0016-5085, 2013, Volume 144, Issue 5, pp. S-1020 - S-1020
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 12/2016, Volume 40, Issue 12, pp. 1601 - 1615
Journal Article
Gastroenterology, ISSN 0016-5085, 2013, Volume 144, Issue 5, pp. 945 - 955.e6
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2016, Volume 11, Issue 8, p. e0156738
Background & Aims The etiology of acute liver failure (ALF) remains elusive in almost half of affected children. We hypothesized that inherited mitochondrial... 
DIAGNOSIS | MITOCHONDRIAL-DNA DEPLETION | RIBONUCLEOTIDE REDUCTASE SUBUNIT | MULTIDISCIPLINARY SCIENCES | DISEASE | ACAD9 | CHOLESTASIS | COMPLEX I DEFICIENCY | MOLECULAR CHARACTERISTICS | MUTATIONS | P53R2 | Liver - pathology | Humans | Liver - metabolism | Child, Preschool | Infant | Male | Liver Failure, Acute - metabolism | Mitochondria - metabolism | Mitochondria - pathology | Genetic Variation | DNA, Mitochondrial - genetics | Energy Metabolism | Mitochondria - genetics | Liver Failure, Acute - genetics | Liver Failure, Acute - pathology | Adolescent | Female | High-Throughput Nucleotide Sequencing | Retrospective Studies | Mutation | Child | Infant, Newborn | Energy metabolism | Liver failure | Care and treatment | Bioenergetics | Patient outcomes | Mitochondrial diseases | Research | Risk factors | Pediatrics | Phosphorylation | Dehydrogenases | Disease | Liver | Genes | Insertion | Pyruvic acid | Mitochondrial DNA | Gene sequencing | Mitochondria | Ribonucleotide reductase | Metabolites | Etiology | Hepatology | Gastroenterology | Genetics | Oxidation | Children | Lactic acidosis | Deoxyribonucleic acid--DNA | Liver diseases | Biochemical analysis | Nutrition | Metabolism | Electron microscopy | Patients | Fatty acids | Steatosis | Genetic variance | Pathology | Hospitals | Hepatocytes | Nitric oxide | Lactic acid | Electron transport | Acidosis | Deoxyribonucleic acid | DNA
Journal Article
Journal Article