von Voss H - Search Results

1

Novel KCNH1 Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of KCNH1-Associated Diseases.

von Wrede R, Jeub M, Ariöz I, Elger CE, von Voss H, Klein HG, Becker AJ, Schoch S, Surges R, Kunz WS. von Wrede R, et al. Among authors: von voss h. Genes (Basel). 2021 Jan 21;12(2):132. doi: 10.3390/genes12020132. Genes (Basel). 2021. PMID: 33494179 Free PMC article.

2

[Acoustic reflexes of children with and without central auditory processing disorders].

Kunze S, Nickisch A, von Voss H, Mall V. Kunze S, et al. Among authors: von voss h. HNO. 2017 Apr;65(4):328-336. doi: 10.1007/s00106-016-0271-2. HNO. 2017. PMID: 27878599 German.

3

[In the discussion about reform of nursing professions the experienced pediatrician has spoken up. In a letter to the Minister of Health Hermann Gröhe expresses his arguments for preservation of pediatric nursing].

Von Voss H. Von Voss H. Kinderkrankenschwester. 2016 May;35(5):184-5. Kinderkrankenschwester. 2016. PMID: 27430057 German. No abstract available.

4

A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum.

Koehler U, Holinski-Feder E, Ertl-Wagner B, Kunz J, von Moers A, von Voss H, Schell-Apacik C. Koehler U, et al. Among authors: von voss h. Eur J Pediatr. 2010 Apr;169(4):463-8. doi: 10.1007/s00431-009-1057-2. Epub 2009 Sep 8. Eur J Pediatr. 2010. PMID: 19763616

5

Maternally inherited heterozygous sequence change in the sonic hedgehog gene in a male patient with bilateral closed-lip schizencephaly and partial absence of the corpus callosum.

Schell-Apacik CC, Ertl-Wagner B, Panzel A, Klausener K, Rausch G, Muenke M, von Voss H, Hehr U. Schell-Apacik CC, et al. Among authors: von voss h. Am J Med Genet A. 2009 Jul;149A(7):1592-4. doi: 10.1002/ajmg.a.32940. Am J Med Genet A. 2009. PMID: 19533790 Free PMC article. No abstract available.

6

Agenesis and dysgenesis of the corpus callosum: clinical, genetic and neuroimaging findings in a series of 41 patients.

Schell-Apacik CC, Wagner K, Bihler M, Ertl-Wagner B, Heinrich U, Klopocki E, Kalscheuer VM, Muenke M, von Voss H. Schell-Apacik CC, et al. Among authors: von voss h. Am J Med Genet A. 2008 Oct 1;146A(19):2501-11. doi: 10.1002/ajmg.a.32476. Am J Med Genet A. 2008. PMID: 18792984 Free PMC article.

7

Pedaudiologic findings after severe neonatal hyperbilirubinemia.

Nickisch A, Massinger C, Ertl-Wagner B, von Voss H. Nickisch A, et al. Among authors: von voss h. Eur Arch Otorhinolaryngol. 2009 Feb;266(2):207-12. doi: 10.1007/s00405-008-0737-2. Epub 2008 Jun 17. Eur Arch Otorhinolaryngol. 2009. PMID: 18560867

8

Conductive education for children with cerebral palsy: effects on hand motor functions relevant to activities of daily living.

Blank R, von Kries R, Hesse S, von Voss H. Blank R, et al. Among authors: von voss h. Arch Phys Med Rehabil. 2008 Feb;89(2):251-9. doi: 10.1016/j.apmr.2007.08.138. Arch Phys Med Rehabil. 2008. PMID: 18226648

9

Expanding the phenotype of alopecia-contractures-dwarfism mental retardation syndrome (ACD syndrome): description of an additional case and review of the literature.

Schell-Apacik C, Hardt M, Ertl-Wagner B, Klopocki E, Möhrenschlager M, Heinrich U, von Voss H. Schell-Apacik C, et al. Among authors: von voss h. Eur J Pediatr. 2008 Sep;167(9):1057-62. doi: 10.1007/s00431-007-0641-6. Epub 2008 Jan 17. Eur J Pediatr. 2008. PMID: 18204861 Review.

10

[MR imaging in congenital disorders of the brain].

Ertl-Wagner B, Rummeny C, von Voss H, Reiser M. Ertl-Wagner B, et al. Among authors: von voss h. Nervenarzt. 2006 Dec;77(12):1521-35; quiz 1536. doi: 10.1007/s00115-006-2188-6. Nervenarzt. 2006. PMID: 17695644 German.

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