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Clinical Genetics|August 26, 1998
Characterization of a novel mutation in exon 10 of the adrenoleukodystrophy geneA Holzinger, E Maier, S Stöckler-Ipsiroglu, et al.
Acta Psychiatrica Scandinavica|January 12, 2011
The loss of sadness: the public's viewA Holzinger, H Matschinger, G Schomerus, et al.
Klinische Padiatrie|August 27, 2009
Congenital Central Hypoventilation Syndrome due to PHOX2b gene defects: inheritance from asymptomatic parentsM Hammel, M Klein, T Trips, et al.
Human Molecular Genetics|April 10, 1999
Adrenoleukodystrophy-related protein can compensate functionally for adrenoleukodystrophy protein deficiency (X-ALD): implications for therapyA Netik, S Forss-Petter, A Holzinger, et al.
Biochemical and Biophysical Research Communications|May 18, 1999
Full length cDNA cloning, promoter sequence, and genomic organization of the human adrenoleukodystrophy related (ALDR) gene functionally redundant to the gene responsible for X-linked adrenoleukodystrophyA Holzinger, P Mayerhofer, J Berger, et al.
Sabouraudia|November 1, 1976
Protothecosis in a cat: first recorded caseW Kaplan, F W Chandler, E A Holzinger, et al.
Prenatal Diagnosis|May 18, 1999
Prenatal diagnosis of X-linked adrenoleukodystrophy combining biochemical, immunocytochemical and DNA analysesE M Maier, A A Roscher, S Kammerer, et al.
Pediatric Research|December 1, 1995
Intraamniotic administration of an adenoviral vector for gene transfer to fetal sheep and mouse tissuesA Holzinger, B C Trapnell, T E Weaver, et al.
Neuropediatrics|April 29, 1998
Clinical and genetic aspects of X-linked adrenoleukodystrophyJ Gärtner, A Braun, A Holzinger, et al.
Acta Psychiatrica Scandinavica|July 13, 2000
Are commonly used self-report inventories suitable for screening postpartum depression and anxiety disorders?M Muzik, C M Klier, K L Rosenblum, et al.
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