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Department of Paediatrics and Adolescent Medicine
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Overview
Publications
(1,223)
Research Grants
(33)
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Journal article
Journal article
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Feasibility, safety and diagnostic impact of endomyocardial biopsies for the diagnosis of myocardial disease in children and adolescents (2018)
Mueller GC, Michel-Behnke I, Knirsch W, Haas NA, Abdul-Khaliq H, Gitter R, Dittrich S, et al.
Journal article
Action Recommendation in accordance with the Guideline "Syncopes in Childhood and Adolescence" (2018)
Dittrich S
Journal article
APPLICATION OF A CENTRAL ILIAC ARTERIOVENOUS COUPLER DEVICE IN SEVERE TREATMENT-RESISTANT ARTERIAL HYPERTENSION: A FOUR-YEAR FOLLOW-UP (2018)
Jung S, Ott C, Karg M, Bosch A, Schmid M, Schlundt C, Achenbach S, Schmieder R
Conference contribution
Systemic-to-pulmonary artery shunting using heparin-bonded grafts (2018)
Ambarsari YA, Purbojo A, Blumauer R, Glöckler M, Toka O, Cesnjevar R, Rueffer A
Journal article
Sweating ability of patients with p63-associated syndromes (2018)
Ferstl P, Wohlfart S, Schneider H
Journal article
Short-term adverse effects of testosterone used for priming in prepubertal boys before growth hormone stimulation test (2018)
Albrecht A, Penger T, Marx M, Hirsch K, Dörr HG
Journal article
Natural history and clinical outcome of junctional epidermolysis bullosa generalized intermediate due to a LAMA3 mutation (2018)
Reimer A, Schwieger-Briel A, He Y, Leppert J, Schauer F, Kiritsi D, Schneider H, et al.
Journal article
Prenatal Correction of X-Linked Hypohidrotic Ectodermal Dysplasia (2018)
Schneider H, Faschingbauer F, Schuepbach-Mallepell S, Koerber I, Wohlfart S, Dick A, Wahlbuhl M, et al.
Journal article
MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia (2018)
Germeshausen M, Ancliff P, Estrada J, Metzler M, Ponstingl E, Ruetschle H, Schwabe D, et al.
Journal article
Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (2018)
Dörr HG, Hess J, Penger T, Marx M, Oppelt P
Journal article
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