151 related articles for article (PubMed ID: 37919484)
1. Cholestatic Liver Disease in a Child with KIF12 Mutation.
Samanta A; Sarma MS; Srivastava A; Poddar U
Indian J Pediatr; 2023 Nov; ():. PubMed ID: 37919484
[TBL] [Abstract][Full Text] [Related]
2. KIF12 Variants and Disturbed Hepatocyte Polarity in Children with a Phenotypic Spectrum of Cholestatic Liver Disease.
Stalke A; Sgodda M; Cantz T; Skawran B; Lainka E; Hartleben B; Baumann U; Pfister ED
J Pediatr; 2022 Jan; 240():284-291.e9. PubMed ID: 34555379
[TBL] [Abstract][Full Text] [Related]
3. Identification of novel loci for pediatric cholestatic liver disease defined by KIF12, PPM1F, USP53, LSR, and WDR83OS pathogenic variants.
Maddirevula S; Alhebbi H; Alqahtani A; Algoufi T; Alsaif HS; Ibrahim N; Abdulwahab F; Barr M; Alzaidan H; Almehaideb A; AlSasi O; Alhashem A; Hussaini HA; Wali S; Alkuraya FS
Genet Med; 2019 May; 21(5):1164-1172. PubMed ID: 30250217
[TBL] [Abstract][Full Text] [Related]
4. Recessive Mutations in
Ünlüsoy Aksu A; Das SK; Nelson-Williams C; Jain D; Özbay Hoşnut F; Evirgen Şahin G; Lifton RP; Vilarinho S
Hepatol Commun; 2019 Apr; 3(4):471-477. PubMed ID: 30976738
[TBL] [Abstract][Full Text] [Related]
5. Panel-Based Next-Generation Sequencing for the Diagnosis of Cholestatic Genetic Liver Diseases: Clinical Utility and Challenges.
Chen HL; Li HY; Wu JF; Wu SH; Chen HL; Yang YH; Hsu YH; Liou BY; Chang MH; Ni YH
J Pediatr; 2019 Feb; 205():153-159.e6. PubMed ID: 30366773
[TBL] [Abstract][Full Text] [Related]
6. Diagnostic yield and novel candidate genes by next generation sequencing in 166 children with intrahepatic cholestasis.
Zheng Y; Guo H; Chen L; Cheng W; Yan K; Zhang Z; Li M; Jin Y; Hu G; Wang C; Zhou C; Zhou W; Jia Z; Zheng B; Liu Z
Hepatol Int; 2024 Apr; 18(2):661-672. PubMed ID: 37314652
[TBL] [Abstract][Full Text] [Related]
7. Progressive familial intrahepatic cholestasis.
Srivastava A
J Clin Exp Hepatol; 2014 Mar; 4(1):25-36. PubMed ID: 25755532
[TBL] [Abstract][Full Text] [Related]
8. MYO5B and bile salt export pump contribute to cholestatic liver disorder in microvillous inclusion disease.
Girard M; Lacaille F; Verkarre V; Mategot R; Feldmann G; Grodet A; Sauvat F; Irtan S; Davit-Spraul A; Jacquemin E; Ruemmele F; Rainteau D; Goulet O; Colomb V; Chardot C; Henrion-Caude A; Debray D
Hepatology; 2014 Jul; 60(1):301-10. PubMed ID: 24375397
[TBL] [Abstract][Full Text] [Related]
9. Enhanced biliary excretion of canalicular membrane enzymes in estrogen-induced and obstructive cholestasis, and effects of different bile acids in the isolated perfused rat liver.
Accatino L; Figueroa C; Pizarro M; Solís N
J Hepatol; 1995 Jun; 22(6):658-70. PubMed ID: 7560859
[TBL] [Abstract][Full Text] [Related]
10. Child with Jaundice and Pruritus: How to Evaluate?
Jagadisan B; Srivastava A
Indian J Pediatr; 2016 Nov; 83(11):1311-1320. PubMed ID: 26932879
[TBL] [Abstract][Full Text] [Related]
11. Diagnostic value of serum gamma-glutamyl transpeptidase activity in liver diseases in children.
Maggiore G; Bernard O; Hadchouel M; Lemonnier A; Alagille D
J Pediatr Gastroenterol Nutr; 1991 Jan; 12(1):21-6. PubMed ID: 1676410
[TBL] [Abstract][Full Text] [Related]
12. Heterozygous mutations of ATP8B1, ABCB11 and ABCB4 cause mild forms of Progressive Familial Intrahepatic Cholestasis in a pediatric cohort.
Mínguez Rodríguez B; Molera Busoms C; Martorell Sampol L; García Romero R; Colomé Rivero G; Martín de Carpi J
Gastroenterol Hepatol; 2022 Oct; 45(8):585-592. PubMed ID: 34942279
[TBL] [Abstract][Full Text] [Related]
13. Diagnostic values of plasma matrix metalloproteinase-7, interleukin-8, and gamma-glutamyl transferase in biliary atresia.
Wu B; Zhou Y; Tian X; Cai W; Xiao Y
Eur J Pediatr; 2022 Nov; 181(11):3945-3953. PubMed ID: 36094664
[TBL] [Abstract][Full Text] [Related]
14. Progressive Familial Intrahepatic Cholestasis: A Study in Children From a Liver Transplant Center in India.
Mehta S; Kumar K; Bhardwaj R; Malhotra S; Goyal N; Sibal A
J Clin Exp Hepatol; 2022; 12(2):454-460. PubMed ID: 35535061
[TBL] [Abstract][Full Text] [Related]
15. A ZFYVE19 gene mutation associated with neonatal cholestasis and cilia dysfunction: case report with a novel pathogenic variant.
Mandato C; Siano MA; Nazzaro L; Gelzo M; Francalanci P; Rizzo F; D'Agostino Y; Morleo M; Brillante S; Weisz A; Franco B; Vajro P
Orphanet J Rare Dis; 2021 Apr; 16(1):179. PubMed ID: 33853651
[TBL] [Abstract][Full Text] [Related]
16. The Mutational Landscape Of Genetic Cholestatic Diseases In Pakistani Children.
Cheema HA; Waheed N; Saeed A; Anjum MN; Fayyaz Z; Ijaz S
J Pak Med Assoc; 2023 Aug; 73(8):1610-1621. PubMed ID: 37697751
[TBL] [Abstract][Full Text] [Related]
17. High hepatic gamma-glutamyltransferase (gamma-GT) activity with normal serum gamma-GT in children with progressive idiopathic cholestasis.
Chobert MN; Bernard O; Bulle F; Lemonnier A; Guellaen G; Alagille D
J Hepatol; 1989 Jan; 8(1):22-5. PubMed ID: 2564009
[TBL] [Abstract][Full Text] [Related]
18. Benign recurrent intrahepatic cholestasis type 2 in a child: A case report and novel mutation.
Akbulut UE; Randa NC; Işık İA; Atalay A
Turk Arch Pediatr; 2021 Jan; 56(1):72-74. PubMed ID: 34013234
[TBL] [Abstract][Full Text] [Related]
19. MYO5B Gene Mutations: A Not Negligible Cause of Intrahepatic Cholestasis of Infancy With Normal Gamma-Glutamyl Transferase Phenotype.
Matarazzo L; Bianco AM; Athanasakis E; Serveres M; Francalanci P; Cenacchi G; Maggiore G; D'Adamo AP
J Pediatr Gastroenterol Nutr; 2022 May; 74(5):e115-e121. PubMed ID: 35129155
[TBL] [Abstract][Full Text] [Related]
20. Genetic contribution of ABCC2 to Dubin-Johnson syndrome and inherited cholestatic disorders.
Corpechot C; Barbu V; Chazouillères O; Broué P; Girard M; Roquelaure B; Chrétien Y; Dong C; Lascols O; Housset C; Jéru I
Liver Int; 2020 Jan; 40(1):163-174. PubMed ID: 31544333
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
