Häussler M - Search Results

1

Tyrosine hydroxylase deficiency causes progressive encephalopathy and dopa-nonresponsive dystonia.

Hoffmann GF, Assmann B, Bräutigam C, Dionisi-Vici C, Häussler M, de Klerk JB, Naumann M, Steenbergen-Spanjers GC, Strassburg HM, Wevers RA. Hoffmann GF, et al. Among authors: haussler m. Ann Neurol. 2003;54 Suppl 6:S56-65. doi: 10.1002/ana.10632. Ann Neurol. 2003. PMID: 12891655

2

L-dopa and selegiline for tyrosine hydroxylase deficiency.

Häussler M, Hoffmann GF, Wevers RA. Häussler M, et al. J Pediatr. 2001 Mar;138(3):451-2. doi: 10.1067/mpd.2001.110776. J Pediatr. 2001. PMID: 11241071 No abstract available.

3

A branch site mutation leading to aberrant splicing of the human tyrosine hydroxylase gene in a child with a severe extrapyramidal movement disorder.

Janssen RJ, Wevers RA, Häussler M, Luyten JA, Steenbergen-Spanjers GC, Hoffmann GF, Nagatsu T, Van den Heuvel LP. Janssen RJ, et al. Among authors: haussler m. Ann Hum Genet. 2000 Sep;64(Pt 5):375-82. doi: 10.1046/j.1469-1809.2000.6450375.x. Ann Hum Genet. 2000. PMID: 11281275

4

Multihandicapped blind and partially sighted children in south Germany. II: Aetiology and pathogenesis.

Häussler M, Bartels H, Strassburg HM. Häussler M, et al. Dev Med Child Neurol. 1996 Dec;38(12):1076-90. doi: 10.1111/j.1469-8749.1996.tb15070.x. Dev Med Child Neurol. 1996. PMID: 8973293

5

Oligoclonal bands predict multiple sclerosis in children with optic neuritis.

Heussinger N, Kontopantelis E, Gburek-Augustat J, Jenke A, Vollrath G, Korinthenberg R, Hofstetter P, Meyer S, Brecht I, Kornek B, Herkenrath P, Schimmel M, Wenner K, Häusler M, Lutz S, Karenfort M, Blaschek A, Smitka M, Karch S, Piepkorn M, Rostasy K, Lücke T, Weber P, Trollmann R, Klepper J, Häussler M, Hofmann R, Weissert R, Merkenschlager A, Buttmann M; for GRACE-MS (German-speaking Research Alliance for ChildrEn with Multiple Sclerosis). Heussinger N, et al. Among authors: haussler m. Ann Neurol. 2015 Jun;77(6):1076-82. doi: 10.1002/ana.24409. Epub 2015 May 11. Ann Neurol. 2015. PMID: 25820181

6

Multihandicapped blind and partially sighted children in south Germany. I: Prevalence, impairments and ophthalmological findings.

Häussler M, Schäfer WD, Neugebauer H. Häussler M, et al. Dev Med Child Neurol. 1996 Dec;38(12):1068-75. doi: 10.1111/j.1469-8749.1996.tb15069.x. Dev Med Child Neurol. 1996. PMID: 8973292

7

[Validity of care assessment in disabled and mentally retarded children].

Häussler M, Streit A, Strassburg HM. Häussler M, et al. Gesundheitswesen. 2002 Oct;64(10):527-33. doi: 10.1055/s-2002-34619. Gesundheitswesen. 2002. PMID: 12375229 German.

8

SIL1 mutations and clinical spectrum in patients with Marinesco-Sjogren syndrome.

Krieger M, Roos A, Stendel C, Claeys KG, Sonmez FM, Baudis M, Bauer P, Bornemann A, de Goede C, Dufke A, Finkel RS, Goebel HH, Häussler M, Kingston H, Kirschner J, Medne L, Muschke P, Rivier F, Rudnik-Schöneborn S, Spengler S, Inzana F, Stanzial F, Benedicenti F, Synofzik M, Lia Taratuto A, Pirra L, Tay SK, Topaloglu H, Uyanik G, Wand D, Williams D, Zerres K, Weis J, Senderek J. Krieger M, et al. Among authors: haussler m. Brain. 2013 Dec;136(Pt 12):3634-44. doi: 10.1093/brain/awt283. Epub 2013 Oct 30. Brain. 2013. PMID: 24176978 Free article.

9

Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study.

Wente S, Schröder S, Buckard J, Büttel HM, von Deimling F, Diener W, Häussler M, Hübschle S, Kinder S, Kurlemann G, Kretzschmar C, Lingen M, Maroske W, Mundt D, Sánchez-Albisua I, Seeger J, Toelle SP, Boltshauser E, Brockmann K. Wente S, et al. Among authors: haussler m. Orphanet J Rare Dis. 2016 Jul 29;11(1):104. doi: 10.1186/s13023-016-0486-z. Orphanet J Rare Dis. 2016. PMID: 27473762 Free PMC article.

10

Genomically anchored vitamin D receptor mediates an abundance of bioprotective actions elicited by its 1,25-dihydroxyvitamin D hormonal ligand.

Haussler MR, Haussler CA, Jurutka PW. Haussler MR, et al. Vitam Horm. 2023;123:313-383. doi: 10.1016/bs.vh.2022.12.008. Epub 2023 Jun 8. Vitam Horm. 2023. PMID: 37717990

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