Häusler M - Search Results

1

Stroke as Initial Manifestation of Adenosine Deaminase 2 Deficiency.

Elbracht M, Mull M, Wagner N, Kuhl C, Abicht A, Kurth I, Tenbrock K, Häusler M. Elbracht M, et al. Among authors: hausler m. Neuropediatrics. 2017 Apr;48(2):111-114. doi: 10.1055/s-0036-1597611. Epub 2016 Dec 26. Neuropediatrics. 2017. PMID: 28024309

2

Early and late onset manifestations of cerebral vasculitis related to varicella zoster.

Häusler MG, Ramaekers VT, Reul J, Meilicke R, Heimann G. Häusler MG, et al. Neuropediatrics. 1998 Aug;29(4):202-7. doi: 10.1055/s-2007-973561. Neuropediatrics. 1998. PMID: 9762696

3

Phenotypic heterogeneity and adverse effects of serine treatment in 3-phosphoglycerate dehydrogenase deficiency: report on two siblings.

Häusler MG, Jaeken J, Mönch E, Ramaekers VT. Häusler MG, et al. Neuropediatrics. 2001 Aug;32(4):191-5. doi: 10.1055/s-2001-17373. Neuropediatrics. 2001. PMID: 11571699

4

Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia.

Bergmann C, Zerres K, Senderek J, Rudnik-Schoneborn S, Eggermann T, Häusler M, Mull M, Ramaekers VT. Bergmann C, et al. Among authors: hausler m. Brain. 2003 Jul;126(Pt 7):1537-44. doi: 10.1093/brain/awg173. Epub 2003 May 21. Brain. 2003. PMID: 12805098 Review.

5

Epilepsy with myoclonic absences - favourable response to add-on rufinamide treatment in 3 cases.

Häusler M, Kluger G, Nikanorova M. Häusler M, et al. Neuropediatrics. 2011 Feb;42(1):28-9. doi: 10.1055/s-0031-1275346. Epub 2011 May 9. Neuropediatrics. 2011. PMID: 21557146

6

Aicardi-Goutières syndrome and systemic lupus erythematosus (SLE) in a 12-year-old boy with SAMHD1 mutations.

Ramantani G, Häusler M, Niggemann P, Wessling B, Guttmann H, Mull M, Tenbrock K, Lee-Kirsch MA. Ramantani G, et al. Among authors: hausler m. J Child Neurol. 2011 Nov;26(11):1425-8. doi: 10.1177/0883073811408310. Epub 2011 Jun 13. J Child Neurol. 2011. PMID: 21670392

7

Early muscle and brain ultrastructural changes in polymerase gamma 1-related encephalomyopathy.

Nolte KW, Trepels-Kottek S, Honnef D, Weis J, Bien CG, van Baalen A, Ritter K, Czermin B, Rudnik-Schöneborn S, Wagner N, Häusler M. Nolte KW, et al. Among authors: hausler m. Neuropathology. 2013 Feb;33(1):59-67. doi: 10.1111/j.1440-1789.2012.01317.x. Epub 2012 Apr 27. Neuropathology. 2013. PMID: 22537151

8

Febrile infection-related epilepsy syndrome without detectable autoantibodies and response to immunotherapy: a case series and discussion of epileptogenesis in FIRES.

van Baalen A, Häusler M, Plecko-Startinig B, Strautmanis J, Vlaho S, Gebhardt B, Rohr A, Abicht A, Kluger G, Stephani U, Probst C, Vincent A, Bien CG. van Baalen A, et al. Among authors: hausler m. Neuropediatrics. 2012 Aug;43(4):209-16. doi: 10.1055/s-0032-1323848. Epub 2012 Aug 21. Neuropediatrics. 2012. PMID: 22911482

9

A Multinational Survey on Actual Diagnostics and Treatment of Subacute Sclerosing Panencephalitis.

Häusler M, Aksoy A, Alber M, Altunbasak S, Angay A, Arsene OT, Craiu D, Hartmann H, Hiz-Kurul S, Ichiyama T, Iliescu C, Jocic-Jakubi B, Korinthenberg R, Köse G, Lukban MB, Ozkan M, Patcheva I, Teichler J, Vintan M, Yaramis A, Yarar C, Yis U, Yuksel D, Anlar B. Häusler M, et al. Neuropediatrics. 2015 Dec;46(6):377-84. doi: 10.1055/s-0035-1564618. Epub 2015 Oct 19. Neuropediatrics. 2015. PMID: 26479761

10

Novel genetic and neuropathological insights in neurogenic muscle weakness, ataxia, and retinitis pigmentosa (NARP).

Claeys KG, Abicht A, Häusler M, Kleinle S, Wiesmann M, Schulz JB, Horvath R, Weis J. Claeys KG, et al. Among authors: hausler m. Muscle Nerve. 2016 Aug;54(2):328-33. doi: 10.1002/mus.25125. Muscle Nerve. 2016. PMID: 27015314

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