Concepedia

Author

Dorothea Möslinger

Medical University of Vienna

Also Known As

D Möslinger, D. Möslinger, Dorothea Möslinger, Dorothea Möslinger, Möslinger, Dorothea

50

Publications

1.2K

Citations

18

H-Index

46

Concepts

All Affiliations

Medical University of ViennaInnsbruck Medical UniversityParacelsus Medical UniversityUniversität InnsbruckUniversity Children's Hospital Zurich
DM

About

Dorothea Möslinger is an author at Medical University of Vienna specializing in medicine, pediatrics, and inherited metabolic disease.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

8

8

264

2

Health Sciences

1

1

55

3

Public Health

1

1

37

4

Epidemiology

1

1

37

5

Family Medicine

1

1

15

Dorothea Möslinger

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22

Publications

1K

Citations

17

H-Index

YearCitations

Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency

Rikke Katrine Jentoft Olsen, Eliška Koňaříková, Teresa Anna Giancaspero,

The American Journal of Human Genetics

2016

146

The natural history of classic galactosemia: lessons from the GalNet registry

M. Estela Rubio‐Gozalbo, Minela Haskovic, Annet M. Bosch,

Orphanet Journal of Rare Diseases

2019

141

3-methylcrotonyl-CoA carboxylase deficiency: Clinical, biochemical, enzymatic and molecular studies in 88 individuals

Sarah C. Grünert, Martin Stucki, Raphael J. Morscher,

Orphanet Journal of Rare Diseases

2012

93

Cross‐sectional observational study of 208 patients with non‐classical urea cycle disorders

Corinne M. Rüegger, Martin Lindner, Diana Ballhausen,

Journal of Inherited Metabolic Disease

2013

77

The National Austrian Newborn Screening Program – Eight years experience with mass spectrometry. Past, present, and future goals

David C. Kasper, Rene Ratschmann, Thomas F. Metz,

Wiener klinische Wochenschrift

2010

68

Estimation of the false-negative rate in newborn screening for congenital adrenal hyperplasia

Felix Votava, Dóra Török, József Kovács,

European Journal of Endocrinology

2005

65

Clinical outcome, biochemical and therapeutic follow-up in 14 Austrian patients with Long-Chain 3-Hydroxy Acyl CoA Dehydrogenase Deficiency (LCHADD)

Daniela Karall, Michaela Brunner‐Krainz, Katharina Kogelnig,

Orphanet Journal of Rare Diseases

2015

58

Clinical and neuropsychological outcome in 33 patients with biotinidase deficiency ascertained by nationwide newborn screening and family studies in Austria

Dorothea Möslinger, Sylvia Stöckler‐Ipsiroglu, S Scheibenreiter,

European Journal of Pediatrics

2001

55

Pompe disease in Austria: clinical, genetic and epidemiological aspects

Wolfgang N. Löscher, Martina Huemer, Thomas M. Stulnig,

Journal of Neurology

2017

37

Reversibility of cirrhotic regenerative liver nodules upon NTBC treatment in a child with tyrosinaemia type I

Julia Crone, Dorothea Möslinger, OA Bodamer,

Acta Paediatrica

2003

36

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