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Items: 1 to 20 of 555

1.

Prematurity Does Not Increase Early Childhood Fracture Risk.

Wagner K, Wagner S, Susi A, Gorman G, Hisle-Gorman E.

J Pediatr. 2018 Dec 7. pii: S0022-3476(18)31605-6. doi: 10.1016/j.jpeds.2018.11.017. [Epub ahead of print]

PMID:
30528571
2.

Role of Liver Biopsy in the Diagnosis of Neonatal Cholestasis due to Biliary Atresia.

Hasan MS, Karim AB, Rukunuzzaman M, Haque A, Akhter MA, Shoma UK, Yasmin F, Rahman MA.

Mymensingh Med J. 2018 Oct;27(4):826-833.

PMID:
30487501
3.

Neonatal Cholestasis: A Primer of Selected Etiologies.

Ananth R.

Pediatr Ann. 2018 Nov 1;47(11):e433-e439. doi: 10.3928/19382359-20181018-01. Review.

PMID:
30423185
4.

Congenital extrahepatic portosystemic shunt: description of four cases and review of the literature.

Ponziani FR, Faccia M, Zocco MA, Giannelli V, Pellicelli A, Ettorre GM, De Matthaeis N, Pizzolante F, De Gaetano AM, Riccardi L, Pompili M, Rapaccini GL.

J Ultrasound. 2018 Oct 24. doi: 10.1007/s40477-018-0329-y. [Epub ahead of print] Review.

PMID:
30357760
5.

Coagulation Disturbances in Patients with Argininemia.

Kiykim E, Zubarioglu T, Cansever MS, Celkan T, Häberle J, Aktuglu Zeybek AC.

Acta Haematol. 2018;140(4):221-225. doi: 10.1159/000493678. Epub 2018 Oct 24.

PMID:
30355940
6.

Association of serum bilirubin in newborns affected by jaundice with gut microbiota dysbiosis.

Zhou S, Wang Z, He F, Qiu H, Wang Y, Wang H, Zhou J, Zhou J, Cheng G, Zhou W, Xu R, Wang M.

J Nutr Biochem. 2019 Jan;63:54-61. doi: 10.1016/j.jnutbio.2018.09.016. Epub 2018 Sep 26.

PMID:
30342317
7.

Cortisol deficiency as a rare cause of neonatal cholestasis.

Lipiński P, Kot K, Jankowska I, Szalecki M.

Dev Period Med. 2018;22(3):280-283.

PMID:
30281525
8.

Inborn Errors of Bile Acid Metabolism.

Heubi JE, Setchell KDR, Bove KE.

Clin Liver Dis. 2018 Nov;22(4):671-687. doi: 10.1016/j.cld.2018.06.006. Epub 2018 Aug 22. Review.

PMID:
30266156
9.

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. 2018 Sep 25. doi: 10.1038/s41436-018-0288-x. [Epub ahead of print]

PMID:
30250217
10.

Diagnostic Accuracy of Serum Matrix Metalloproteinase-7 for Biliary Atresia.

Yang L, Zhou Y, Xu PP, Mourya R, Lei HY, Cao GQ, Xiong XL, Xu H, Duan XF, Wang N, Fei L, Chang XP, Zhang X, Jiang M, Bezerra JA, Tang ST.

Hepatology. 2018 Dec;68(6):2069-2077. doi: 10.1002/hep.30234. Epub 2018 Nov 15.

PMID:
30153340
11.

Arthrogryposis, renal dysfunction and cholestasis (ARC) syndrome: a rare association with high GGT level and absent kidney.

Gupta V, Pandita A, Panghal A, Kallem V.

BMJ Case Rep. 2018 Aug 9;2018. pii: bcr-2017-223715. doi: 10.1136/bcr-2017-223715.

PMID:
30093463
12.

Development and Validation of Novel Diagnostic Models for Biliary Atresia in a Large Cohort of Chinese Patients.

Dong R, Jiang J, Zhang S, Shen Z, Chen G, Huang Y, Zheng Y, Zheng S.

EBioMedicine. 2018 Aug;34:223-230. doi: 10.1016/j.ebiom.2018.07.025. Epub 2018 Aug 1.

13.

Clinical Assessment of Differential Diagnostic Methods in Infants with Cholestasis due to Biliary Atresia or Non-Biliary Atresia.

Dong C, Zhu HY, Chen YC, Luo XP, Huang ZH.

Curr Med Sci. 2018 Feb;38(1):137-143. doi: 10.1007/s11596-018-1857-6. Epub 2018 Mar 15.

PMID:
30074163
14.

Outcomes of Alagille syndrome following the Kasai operation: a systematic review and meta-analysis.

Fujishiro J, Suzuki K, Watanabe M, Uotani C, Takezoe T, Takamoto N, Hayashi K.

Pediatr Surg Int. 2018 Oct;34(10):1073-1077. doi: 10.1007/s00383-018-4316-3. Epub 2018 Aug 2. Review.

PMID:
30073479
15.

Severe Neonatal Cholestasis as an Early Presentation of McCune Albright Syndrome.

Coles N, Comeau I, Munoz T, Harrington J, Mendoza-Londono R, Schulze A, Kives S, Kamath BM, Hamilton J.

J Clin Res Pediatr Endocrinol. 2018 Jul 11. doi: 10.4274/jcrpe.0110. [Epub ahead of print]

16.

Reduced Hepatocellular Expression of Canalicular Transport Proteins in Infants with Neonatal Cholestasis and Congenital Hypopituitarism.

Grammatikopoulos T, Deheragoda M, Strautnieks S, Neves Souza L, Hinds R, Thompson RJ, Hadzic N.

J Pediatr. 2018 Sep;200:181-187. doi: 10.1016/j.jpeds.2018.05.009. Epub 2018 Jun 20.

PMID:
29935878
17.

Serum level of interleukin-13 receptor alpha 2 in infants with biliary atresia - is it of value?

Adawy N, El-Araby H, Allam A, Elshenawy S, Khedr M, Ibrahim Y, Zakaria HM.

Clin Exp Hepatol. 2018 Jun;4(2):91-96. doi: 10.5114/ceh.2018.75958. Epub 2018 May 25.

18.

Correlation of APRI Index with Metavir Index in Children with Neonatal Cholestasis Without Biliary Atresia.

Shah I, Madgum N.

Ann Hepatol. 2018 July - August ,;17(4):592-595. doi: 10.5604/01.3001.0012.0924.

19.

Pathologic Features of Hereditary Cholestatic Diseases.

Clouston AD.

Surg Pathol Clin. 2018 Jun;11(2):313-327. doi: 10.1016/j.path.2018.02.001. Epub 2018 Mar 26. Review.

PMID:
29751877
20.

Germline Hemizygous Deletion of Gene HNF1B Associated with a Case of Severe Neonatal Cholestasis and Hepatocarcinoma.

de Leusse C, De Paula AM, Ascherod A, Parache C, Geraldine H, Cailliez M, Missirian C, Fabre A.

J Pediatr Gastroenterol Nutr. 2018 Apr 27. doi: 10.1097/MPG.0000000000002015. [Epub ahead of print] No abstract available.

PMID:
29727438

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