Publications by authors named "Martin LaaSS"

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Paediatric acute liver failure: A prospective, nationwide, population-based surveillance study in Germany.
Dominic Lenz, Muhammad Abdulaziz, Bianca Peters, Matias Wagner, Lea D Schlieben, Martin Laass

J Pediatr Gastroenterol Nutr· September 2025

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Hepatic Phenotype in NBAS-Associated Disease: Clinical Course, Prognostic Factors and Outcome in 230 Patients.
Bianca Peters, Lea Dewi Schlieben, Heiko Brennenstuhl, Cigdem Arikan, Sarah M Bedoyan

Liver Int· July 2025

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Compassionate Use of Osocimab in Preventing Thrombotic Complications Without Incremental Bleeding: A Case Report.
Jan Beyer-Westendorf, Katrin Weber, Falk Eckart, Martin W Laass, Ralf Knöfler

TH Open· May 2025

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Genetic landscape of pediatric acute liver failure of indeterminate origin.
Dominic Lenz, Lea D Schlieben, Masaru Shimura, Alyssa Bianzano, Dmitrii Smirnov, Martin W Laass

Hepatology· May 2024

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Impact of genetic and non-genetic factors on phenotypic diversity in NBAS-associated disease.
Nicole Hammann, Dominic Lenz, Ivo Baric, Ellen Crushell, Carlo Dionisi Vici, Martin W Laass

Mol Genet Metab· March 2024

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Growth development of children and adolescents with inflammatory bowel disease in the period 2000-2014 based on data of the Saxon pediatric IBD registry: a population-based study.
Xueming Zhou, Ivana Kern, Ulrike Rothe, Olaf Schoffer, Jens Weidner, Martin W Laass

BMC Gastroenterol· January 2024

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Metamizole-induced agranulocytosis (MIA): a mini review.
Markos K Tomidis Chatzimanouil, Ines Goppelt, Yvonne Zeissig, Ulrich J Sachs, Martin W Laass

Mol Cell Pediatr· August 2023

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Clinical course of new-onset Crohn's disease in children and adolescents in dependency of age, initial location, initial severity level and therapy over the period 2000-2014 based on the Saxon Pediatric IBD-Registry in Germany.
Fan Dong, Ivana Kern, Jens Weidner, Kathleen Kügler, Ulrike Rothe

PLoS One· July 2023

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Novel mutation and expanding phenotype in IRF2BP2 deficiency.
Julia Körholz, Anastasia Gabrielyan, Henrike Lisa Sczakiel, Livia Schulze, Manuela Rejzek, Martin W Laass

Rheumatology (Oxford)· April 2023

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Human glycoprotein-2 expressed in Brunner glands - A putative autoimmune target and link between Crohn's and coeliac disease.
Dirk Roggenbuck, Alexander Goihl, Mandy Sowa, Steffi Lopens, Stefan Rödiger, Martin W Laass

Clin Immunol· February 2023

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[Chronic or severe enteropathy and immunodeficiency: be prepared for a rara avis].
Katrin Weber, Yvonne Zeißig, Cornelie Haag, Renate Schmelz, Julia Pazmandi, Martin W Laass

Z Gastroenterol· November 2022

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PR3-ANCAs Detected by Third-Generation ELISA Predicts Severe Disease and Poor Survival in Primary Sclerosing Cholangitis.
Steffi Lopens, Ewa Wunsch, Malgorzata Milkiewicz, Nadja Röber, Grit Zarske, Martin Laass

Diagnostics (Basel)· November 2022

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Current and projected incidence trends of pediatric-onset inflammatory bowel disease in Germany based on the Saxon Pediatric IBD Registry 2000-2014 -a 15-year evaluation of trends.
Ivana Kern, Olaf Schoffer, Thomas Richter, Wieland Kiess, Gunter Flemming, Martin W Laass

PLoS One· September 2022

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Hyper-IgE and Carcinoma in CADINS Disease.
Leonora Pietzsch, Julia Körholz, Felix Boschann, Mildred Sergon, Batsukh Dorjbal, Martin W Laass

Front Immunol· June 2022

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Occurrence of Thromboembolism in Paediatric Patients With Inflammatory Bowel Disease: Data From the CEDATA-GPGE Registry.
Jan De Laffolie, Antje Ballauff, Stefan Wirth, Carolin Blueml, Frank Risto Rommel

Front Pediatr· June 2022

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[Not Available].
Jörg Felber, Hendrik Bläker, Wolfgang Fischbach, Sibylle Koletzko, Martin Laaß

Z Gastroenterol· May 2022

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Anti-Proteinase 3 Antibodies as a Biomarker for Ulcerative Colitis and Primary Sclerosing Cholangitis in Children.
Martin Walter Laass, Josefine Ziesmann, Jan de Laffolie, Nadja Röber, Karsten Conrad

J Pediatr Gastroenterol Nutr· April 2022

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Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects.
Andreas R Janecke, Xiaoqin Liu, Rüdiger Adam, Sumanth Punuru, Arne Viestenz, Martin Laass

Hum Genet· August 2021

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Incidence trends of pediatric onset inflammatory bowel disease in the years 2000-2009 in Saxony, Germany-first results of the Saxon Pediatric IBD Registry.
Ivana Kern, Olaf Schoffer, Wieland Kiess, Jobst Henker, Martin W Laaß

PLoS One· April 2021

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Defining clinical subgroups and genotype-phenotype correlations in NBAS-associated disease across 110 patients.
Christian Staufner, Bianca Peters, Matias Wagner, Seham Alameer, Ivo Barić, Martin W Laass

Genet Med· March 2020

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Orbital inflammation and colitis in pediatric IgG4-related disease: A case report and review of the literature.
Lissy Tille, Anja Schnabel, Martin W Laass, Gabriele Hahn, Heike Taut

Eur J Rheumatol· February 2020

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Mutations in RPSA and NKX2-3 link development of the spleen and intestinal vasculature.
Chantal Kerkhofs, Servi J C Stevens, Saul N Faust, William Rae, Anthony P Williams, Martin Laass

Hum Mutat· January 2020

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Identification of Chitinase-3-Like Protein 1 as a Novel Neutrophil Antigenic Target in Crohn's Disease.
Claudia Deutschmann, Mandy Sowa, Jayaseelan Murugaiyan, Uwe Roesler, Nadja Röber, Martin W Laass

J Crohns Colitis· July 2019

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Novel VPS33B mutation in a patient with autosomal recessive keratoderma-ichthyosis-deafness syndrome.
Svenja Alter, Alrun Hotz, Arne Jahn, Nataliya Di Donato, Evelin Schröck, Martin W Laass

Am J Med Genet A· December 2018

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School-related experience and performance with inflammatory bowel disease: results from a cross-sectional survey in 675 children and their parents.
Magdalena Freckmann, Alexander Seipp, Martin W Laass, Sibylle Koletzko, Martin Claßen

BMJ Open Gastroenterol· November 2018

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