Weigell-Weber M - Search Results

1

DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland.

Laccone F, Engel U, Holinski-Feder E, Weigell-Weber M, Marczinek K, Nolte D, Morris-Rosendahl DJ, Zühlke C, Fuchs K, Weirich-Schwaiger H, Schlüter G, von Beust G, Vieira-Saecker AM, Weber BH, Riess O. Laccone F, et al. Among authors: weigell weber m. Neurology. 1999 Sep 11;53(4):801-6. doi: 10.1212/wnl.53.4.801. Neurology. 1999. PMID: 10489044

2

Psychiatric symptoms and CAG expansion in Huntington's disease.

Weigell-Weber M, Schmid W, Spiegel R. Weigell-Weber M, et al. Am J Med Genet. 1996 Feb 16;67(1):53-7. doi: 10.1002/(SICI)1096-8628(19960216)67:1<53::AID-AJMG9>3.0.CO;2-T. Am J Med Genet. 1996. PMID: 8678115

3

Striatal glucose metabolism and dopamine D2 receptor binding in asymptomatic gene carriers and patients with Huntington's disease.

Antonini A, Leenders KL, Spiegel R, Meier D, Vontobel P, Weigell-Weber M, Sanchez-Pernaute R, de Yébenez JG, Boesiger P, Weindl A, Maguire RP. Antonini A, et al. Among authors: weigell weber m. Brain. 1996 Dec;119 ( Pt 6):2085-95. doi: 10.1093/brain/119.6.2085. Brain. 1996. PMID: 9010012 Free article.

4

[Direct genetic diagnosis in Huntington's chorea].

Spiegel R, Weigell-Weber M, Hergersberg M, Schmid W. Spiegel R, et al. Schweiz Med Wochenschr. 1993 Dec 4;123(48):2271-7. Schweiz Med Wochenschr. 1993. PMID: 8272801 Review. German.

5

Genetic heterogeneity in autosomal dominant pattern dystrophy of the retina.

Weigell-Weber M, Kryenbühl C, Büchi ER, Spiegel R. Weigell-Weber M, et al. Mol Vis. 1996 Jun 20;2:6. Mol Vis. 1996. PMID: 9238083 Free article.

6

A novel complex mutation event in the peripherin/RDS gene in a family with retinal pattern dystrophy.

Pajic B, Weigell-Weber M, Schipper I, Kryenbühl C, Büchi ER, Spiegel R, Hergersberg M. Pajic B, et al. Among authors: weigell weber m. Retina. 2006 Oct;26(8):947-53. doi: 10.1097/01.iae.0000250010.60908.e3. Retina. 2006. PMID: 17031298

7

McLeod syndrome: a novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings.

Jung HH, Hergersberg M, Kneifel S, Alkadhi H, Schiess R, Weigell-Weber M, Daniels G, Kollias S, Hess K. Jung HH, et al. Among authors: weigell weber m. Ann Neurol. 2001 Mar;49(3):384-92. Ann Neurol. 2001. PMID: 11261514

8

Genomewide homozygosity mapping and molecular analysis of a candidate gene located on 22q13 (fibulin-1) in a previously undescribed vitreoretinal dystrophy.

Weigell-Weber M, Sarra GM, Kotzot D, Sandkuijl L, Messmer E, Hergersberg M. Weigell-Weber M, et al. Arch Ophthalmol. 2003 Aug;121(8):1184-8. doi: 10.1001/archopht.121.8.1184. Arch Ophthalmol. 2003. PMID: 12912698 Free article.

9

[Hereditary hearing loss: new diagnostic possibilities].

Hergersberg M, Weigell-Weber M. Hergersberg M, et al. Among authors: weigell weber m. Schweiz Med Wochenschr. 2000 Apr 1;130(13):485-9. Schweiz Med Wochenschr. 2000. PMID: 10812644 German.

10

[Hereditary hearing loss due to mutations in the connexin-26 gene].

Weigell-Weber M, Schinzel A, Hergersberg M. Weigell-Weber M, et al. Schweiz Med Wochenschr. 2000 Jul 25;130(29-30):1072-7. Schweiz Med Wochenschr. 2000. PMID: 10971940 German.

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