Prof. Dr. med. Heiko Martin Reutter



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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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Abstract

Journal

SIADH as presenting feature of foramen magnum stenosis in a 2-month-old infant with achondroplasia (ACH): case report and discussion on management of infants with ACH in order to reduce the risk of serious complications (2022) Cebeci AN, Hébert S, Reutter HM, Wölfle J Conference contribution Brain Abnormalities in Patients with Germline Variants in H3F3: Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors (2022) Alves CA, Sherbini O, D’Arco F, Steel D, Kurian MA, Radio FC, Ferrero GB, et al. Journal article Definition, diagnosis and clinical management of non-obstructive kidney dysplasia: a consensus statement by the ERKNet Working Group on Kidney Malformations (2022) Kohl S, Avni FE, Boor P, Capone V, Clapp WL, De Palma D, Harris T, et al. Journal article Exome sequencing in individuals with cardiovascular laterality defects identifies potential candidate genes (2022) Breuer K, Riedhammer KM, Mueller N, Schaidinger B, Dombrowsky G, Dittrich S, Zeidler S, et al. Journal article First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B (2022) Gehlen J, Giel AS, Köllges R, Haas SL, Zhang R, Trcka J, Sungur A, et al. Journal article Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge (2022) Brosens E, Peters NC, van Weelden KS, Bendixen C, Brouwer RW, Sleutels F, Bruggenwirth HT, et al. Journal article, Review article Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT4 in the formation of primary congenital chylothorax (2022) Schneider S, Kollges R, Stegmann JD, Thieme F, Hilger AC, Waffenschmidt L, Fazaal J, et al. Journal article, Letter Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores (2022) Ishorst N, Henschel L, Thieme F, Drichel D, Sivalingam S, Mehrem SL, Fechtner AC, et al. Journal article Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations (2022) Fabian J, Dworschak GC, Waffenschmidt L, Schierbaum L, Bendixen C, Heilmann-Heimbach S, Sivalingam S, et al. Journal article Blood pressure and kidney function in neonates and young infants with intrauterine growth restriction (2022) Heuchel KM, Ebach F, Alsat EA, Reutter HM, Mueller A, Hilger AC Journal article
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