Evaluation of a Recently Established Test for Familial Hyperaldosteronism Type 1
Dringenberg, T, Sorokina, M, Ehlers, M, Dekomien, G, Haase, M, Schulze, E, Quinkler, M, Rump, L C, Schott, M, Willenberg, H S
Published in Hormone and metabolic research (01.12.2016)
Published in Hormone and metabolic research (01.12.2016)
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Journal Article
Autosomal dominant nemaline myopathy caused by a novel α-tropomyosin 3 mutation
Kiphuth, I. C., Krause, S., Huttner, H. B., Dekomien, G., Struffert, T., Schröder, R.
Published in Journal of neurology (01.04.2010)
Published in Journal of neurology (01.04.2010)
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Journal Article
Substrate deprivation therapy in juvenile Sandhoff disease
Wortmann, S. B., Lefeber, D. J., Dekomien, G., Willemsen, M. A. A. P., Wevers, R. A., Morava, E.
Published in Journal of inherited metabolic disease (01.12.2009)
Published in Journal of inherited metabolic disease (01.12.2009)
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Journal Article
New cases of adult-onset Sandhoff disease with a cerebellar or lower motor neuron phenotype
Delnooz, C C S, Lefeber, D J, Langemeijer, S M C, Hoffjan, S, Dekomien, G, Zwarts, M J, Van Engelen, B G M, Wevers, R A, Schelhaas, H J, van de Warrenburg, B P C
Published in Journal of neurology, neurosurgery and psychiatry (01.09.2010)
Published in Journal of neurology, neurosurgery and psychiatry (01.09.2010)
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Journal Article
Rapid genetic diversification within dog breeds as evidenced by a case study on Schnauzers
Streitberger, K., Schweizer, M., Kropatsch, R., Dekomien, G., Distl, O., Fischer, M. S., Epplen, J. T., Hertwig, S. T.
Published in Animal genetics (01.10.2012)
Published in Animal genetics (01.10.2012)
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Journal Article
Mutations in the calcium-sensing receptor: a new genetic risk factor for chronic pancreatitis?
Felderbauer, P, Klein, W, Bulut, K, Ansorge, N, Dekomien, G, Werner, I, Epplen, J T, Schmitz, F, Schmidt, W E
Published in Scandinavian journal of gastroenterology (01.03.2006)
Published in Scandinavian journal of gastroenterology (01.03.2006)
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Journal Article
Identification of a tyrosinase (TYR) exon 4 deletion in albino ferrets (Mustela putorius furo)
Blaszczyk, W.M, Distler, C, Dekomien, G, Arning, L, Hoffmann, K.-P, Epplen, J.T
Published in Animal genetics (01.08.2007)
Published in Animal genetics (01.08.2007)
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Journal Article
The LRRK2 gene in Parkinson’s disease: mutation screening in patients from Germany
Schlitter, A M, Woitalla, D, Mueller, T, Epplen, J T, Dekomien, G
Published in Journal of neurology, neurosurgery and psychiatry (01.07.2006)
Published in Journal of neurology, neurosurgery and psychiatry (01.07.2006)
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Journal Article
Inclusion body myositis, Paget's disease of the bone and frontotemporal dementia: early involvement of the heart and respiratory muscles
Ponfick, M, Ludolph, A C, Dekomien, G, Uttner, I, Kassubek, J, Gdynia, H-J
Published in Fortschritte der Neurologie-Psychiatrie (01.06.2012)
Published in Fortschritte der Neurologie-Psychiatrie (01.06.2012)
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Journal Article
On ancestors of dog breeds with focus on Weimaraner hunting dogs
Kropatsch, R, Streitberger, K, Schulte-Middelmann, T, Dekomien, G, Epplen, J.T
Published in Journal of animal breeding and genetics (1986) (01.02.2011)
Published in Journal of animal breeding and genetics (1986) (01.02.2011)
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Journal Article
Tracing the origin of ‘blue Weimaraner' dogs by molecular genetics
Gerding, W.M, Schreiber, S, Dekomien, G, Epplen, J.T
Published in Journal of animal breeding and genetics (1986) (01.04.2011)
Published in Journal of animal breeding and genetics (1986) (01.04.2011)
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Journal Article
Generalized progressive retinal atrophy of sloughi dogs is due to an 8-bp insertion in exon 21 of the PDE6B gene
DEKOMIEN, G, RUNTE, M, GÖDDE, R, EPPLEN, J. T
Published in Cytogenetic and genome research (01.01.2000)
Published in Cytogenetic and genome research (01.01.2000)
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Journal Article
G.P.10.02 Does δ-sarcoglycan-associated autosomal dominant cardiomyopathy exist?
Sarkozy, A, Bauer, R, Hudson, J, Müller, H.D, Sommer, C, Dekomien, G, Bourke, J, Routledge, D, Bushby, K, Klepper, J, Straub, V
Published in Neuromuscular disorders : NMD (01.09.2009)
Published in Neuromuscular disorders : NMD (01.09.2009)
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Journal Article
Gene symbol: RYR1. Disease: malignant hyperthermia
Dekomien, G, Gencik, M, Gencikova, A, Klenk, Y, Epplen, J T
Published in Human genetics (01.12.2005)
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Published in Human genetics (01.12.2005)
Journal Article
Gene symbol: RYR1. Disease: malignant hyperthermia
Dekomien, G, Gencik, M, Gencikova, A, Klenk, Y, Epplen, J T
Published in Human genetics (01.12.2005)
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Published in Human genetics (01.12.2005)
Journal Article
Pancreatitis in primary hyperparathyroidism-related hypercalcaemia is not associated with mutations in the CASR gene
Felderbauer, P, Karakas, E, Fendrich, V, Bulut, K, Werner, I, Dekomien, G, Klein, W, Bartsch, D, Schmidt, W E
Published in Experimental and clinical endocrinology & diabetes (01.09.2007)
Published in Experimental and clinical endocrinology & diabetes (01.09.2007)
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Journal Article
Gene symbol: RYR1. Disease: malignant hyperthermia
Dekomien, G, Gencik, M, Gencikova, A, Klenk, Y, Epplen, J T
Published in Human genetics (01.12.2005)
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Published in Human genetics (01.12.2005)
Journal Article
Alpha vs. gamma sarcoglycanopathy: DNA tests solve a case from Argentina
Avila De Salman, S, Taratuto, A L, Dekomien, G, Carrero-Valenzuela, R
Published in Acta myologica (01.10.2007)
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Published in Acta myologica (01.10.2007)
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