Detalhe da pesquisa
1.
Microbiome analysis and fecal microbiota transfer in pediatric gastroenterology - a structured online survey in German-speaking countries.
Int J Colorectal Dis
; 38(1): 59, 2023 Mar 03.
Artigo
Inglês
| MEDLINE | ID: mdl-36867263
2.
The Role of Psychotherapy in the Care of Patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.
Medicina (Kaunas)
; 59(4)2023 Apr 06.
Artigo
Inglês
| MEDLINE | ID: mdl-37109676
3.
Spasmodic Abdominal Pain and Other Gastrointestinal Symptoms in Pontocerebellar Hypoplasia Type 2.
Neuropediatrics
; 52(6): 495-498, 2021 12.
Artigo
Inglês
| MEDLINE | ID: mdl-34255333
4.
CCDC115 Deficiency Causes a Disorder of Golgi Homeostasis with Abnormal Protein Glycosylation.
Am J Hum Genet
; 98(2): 310-21, 2016 Feb 04.
Artigo
Inglês
| MEDLINE | ID: mdl-26833332
5.
[Health damages after ingestion of button batteries in childhood]. / Gesundheitsschäden nach Ingestion von Knopfzellbatterien im Kindesalter.
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz
; 62(11): 1354-1361, 2019 Nov.
Artigo
Alemão
| MEDLINE | ID: mdl-31620820
6.
An inducible mouse model for microvillus inclusion disease reveals a role for myosin Vb in apical and basolateral trafficking.
Proc Natl Acad Sci U S A
; 112(40): 12408-13, 2015 Oct 06.
Artigo
Inglês
| MEDLINE | ID: mdl-26392529
7.
[The overview of the current evidence ignores the current evidence]. / Die Übersicht zur aktuellen Evidenz ignoriert die aktuelle Evidenz.
Nervenarzt
; 94(8): 736-737, 2023 08.
Artigo
Alemão
| MEDLINE | ID: mdl-37368011
8.
Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrhea.
Hum Mol Genet
; 24(23): 6614-23, 2015 Dec 01.
Artigo
Inglês
| MEDLINE | ID: mdl-26358773
9.
Bile salt export pump-reactive antibodies form a polyclonal, multi-inhibitory response in antibody-induced bile salt export pump deficiency.
Hepatology
; 63(2): 524-37, 2016 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-26516723
10.
Pediatric gastrointestinal endoscopy: European Society of Gastrointestinal Endoscopy (ESGE) and European Society for Paediatric Gastroenterology Hepatology and Nutrition (ESPGHAN) Guideline Executive summary.
Endoscopy
; 49(1): 83-91, 2017 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-27617420
11.
Inflammatory bowel disease caused by primary immunodeficiencies-Clinical presentations, review of literature, and proposal of a rational diagnostic algorithm.
Pediatr Allergy Immunol
; 28(5): 412-429, 2017 08.
Artigo
Inglês
| MEDLINE | ID: mdl-28513998
12.
Paediatric Gastrointestinal Endoscopy: European Society for Paediatric Gastroenterology Hepatology and Nutrition and European Society of Gastrointestinal Endoscopy Guidelines.
J Pediatr Gastroenterol Nutr
; 64(1): 133-153, 2017 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27622898
13.
Mitochondrial dysfunction in liver failure requiring transplantation.
J Inherit Metab Dis
; 39(3): 427-436, 2016 05.
Artigo
Inglês
| MEDLINE | ID: mdl-27053192
14.
Etiology, outcome and prognostic factors of childhood acute liver failure in a German Single Center.
Ann Hepatol
; 14(5): 722-8, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-26256901
15.
Pulse oximetry is insufficient for timely diagnosis of hepatopulmonary syndrome in children with liver cirrhosis.
J Pediatr
; 164(3): 546-52.e1-2, 2014 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-24321540
16.
Spectrum of pathogens in native liver, bile, and blood during pediatric liver transplantation.
Pediatr Transplant
; 18(3): 266-71, 2014 May.
Artigo
Inglês
| MEDLINE | ID: mdl-24597705
17.
Liver cirrhosis in glycogen storage disease Ib.
Mol Genet Metab
; 108(3): 198-200, 2013 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-23357201
18.
Gilbert's syndrome--a frequent cause of unconjugated hyperbilirubinemia in children after orthotopic liver transplantation.
Pediatr Transplant
; 16(2): 201-4, 2012 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-22360405
19.
Prevalence of hepatitis E virus infection in pediatric solid organ transplant recipients--a single-center experience.
Pediatr Transplant
; 16(7): 742-7, 2012 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-22738211
20.
Acute liver failure with subsequent cirrhosis as the primary manifestation of TRMU mutations.
J Inherit Metab Dis
; 34(1): 197-201, 2011 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-21153446