T M Neuhann
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Explore the profile of T M Neuhann including associated specialties, affiliations and a list of published articles.
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Articles
6
Citations
25
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0
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Recent Articles
1.
Neuhann T
Klin Monbl Augenheilkd
. 2015 Feb;
232(3):259-65.
PMID: 25654236
If not due to trauma, ectopia lentis is usually caused genetically. It is a main symptom of several syndromal disorders such as Marfan syndrome or homocystinuria. Also other connective tissue...
2.
Nowidi K, Kunisch R, Bouna-Pyrrou P, Meissner D, Hennig-Fast K, Weindl A, et al.
Fortschr Neurol Psychiatr
. 2013 Apr;
81(6):337-45.
PMID: 23612984
We report upon a case of a 55 year old patient with a bipolar affective disorder, presenting herself with a depressive symptomatology in addition to a severe motor perturbation. The...
3.
Neuhann T, Muller D, Hackmann K, Holzinger S, Schrock E, Di Donato N
Eur J Med Genet
. 2012 Apr;
55(6-7):423-8.
PMID: 22469822
We report on a male patient with the proposed diagnosis of the rare but very distinct entity of van Maldergem syndrome. His parents are first cousins. At the age of...
4.
Tyshchenko N, Neuhann T, Gerlach E, Hahn G, Heisch K, Rump A, et al.
Am J Med Genet A
. 2011 Aug;
155A(9):2060-5.
PMID: 21834043
We report on three patients from two families with apparently a novel clinical entity. The main features of which include unusual craniofacial dysmorphism with ptosis, prominent eyes, flat midface, Cupid's...
5.
Gerber J, Neuhann T, Tyshchenko N, Smitka M, Hackmann K
Am J Med Genet A
. 2011 Jul;
155A(8):1981-6.
PMID: 21744487
Subtelomeric deletions of chromosome 6q may result in a syndrome with brain malformations, comprising hydrocephalus and hypoplasia of the corpus callosum. Aplasia of the olfactory bulbs (OB) or anosmia has...
6.
Rauscher C, Poretti A, Neuhann T, Forstner R, Hahn G, Koch J, et al.
Neuropediatrics
. 2009 Jul;
40(1):43-6.
PMID: 19639528
Pontine tegmental cap dysplasia (PTCD) is a newly described hindbrain malformation with distinct neuroradiological findings. Only 12 cases of PTCD have been described so far, all sporadic. We report 2...