S. Straub

Early onset systemic lupus erythematosus: differential diagnoses, clinical presentation, and treatment options

M. Gahr, G. Heubner, K. Wieczorek, 2011, Clinical Rheumatology.

Stereotactic radiofrequency ablation of a variety of liver masses in children

R. Bale, R. Crazzolara, B. Meister, 2020, International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group.

A novel therapeutic approach for LPIN1 mutation–associated rhabdomyolysis—The Austrian experience

J. Zschocke, D. Karall, R. Birnbacher, 2015, Muscle & nerve.

Biallelic IARS Mutations Cause Growth Retardation with Prenatal Onset, Intellectual Disability, Muscular Hypotonia, and Infantile Hepatopathy.

M. Carl, I. Harting, T. Meitinger, 2016, American journal of human genetics.

Intestinal microvascular malformations and congenital asplenia in an adolescent possibly expanding the phenotype of Ivemark syndrome.

D. Aust, F. Hauck, C. Würfel, 2011, European journal of gastroenterology & hepatology.

Effectiveness and safety of ferric carboxymaltose treatment in children and adolescents with inflammatory bowel disease and other gastrointestinal diseases

G. Virgin, T. Cushway, M. Laass, 2014, BMC Gastroenterology.

Internal Ileal Diversion as Treatment for Progressive Familial Intrahepatic Cholestasis Type 1-Associated Graft Inflammation and Steatosis after Liver Transplantation

F. Messner, S. Schneeberger, A. Janecke, 2022, Children.

Co-existence of ABCB11 and DCDC2 disease: Infantile cholestasis requires both next-generation sequencing and clinical-histopathologic correlation

A. Janecke, T. Müller, Georg F. Vogel, 2020, European Journal of Human Genetics.

Gastric outlet obstruction in a 5-year-old boy: Heineke-Mikulicz pyloroplasty is curative

P. Hechenleitner, M. Sanal, O. Renz, 2017 .