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Literature DB >> 25970799

Mutations in HTRA2 are not a common cause of familial classic ET.

Franziska Hopfner¹, Stefanie H Müller¹, Delia Lorenz¹, Silke Appenzeller², Stephan Klebe³, Günther Deuschl¹, Gregor Kuhlenbäumer¹.

Abstract

Entities: Gene

Mesh：

Substances：

Year: 2015 PMID： 25970799 DOI： 10.1002/mds.26252

Source DB: PubMed Journal: Mov Disord ISSN： 0885-3185 Impact factor: 10.338

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6 in total

1. Cerebellar Pathology in Familial vs. Sporadic Essential Tremor.

Authors: Elan D Louis; Sheng-Han Kuo; Jie Wang; William J Tate; Ming-Kai Pan; Geoffrey C Kelly; Jesus Gutierrez; Etty P Cortes; Jean-Paul G Vonsattel; Phyllis L Faust
Journal: Cerebellum Date: 2017-08 Impact factor: 3.847

Review 2. Knowledge gaps and research recommendations for essential tremor.

Authors: Franziska Hopfner; Dietrich Haubenberger; Wendy R Galpern; Katrina Gwinn; Ashlee Van't Veer; Samantha White; Kailash Bhatia; Charles H Adler; David Eidelberg; William Ondo; Glenn T Stebbins; Caroline M Tanner; Rick C Helmich; Fred A Lenz; Roy V Sillitoe; David Vaillancourt; Jerrold L Vitek; Elan D Louis; Holly A Shill; Matthew P Frosch; Tatiana Foroud; Gregor Kuhlenbäumer; Andrew Singleton; Claudia M Testa; Mark Hallett; Rodger Elble; Günther Deuschl
Journal: Parkinsonism Relat Disord Date: 2016-10-04 Impact factor: 4.891

Mutations in HTRA2 are not a common cause of familial classic ET.

1. Cerebellar Pathology in Familial vs. Sporadic Essential Tremor.

Review 2. Knowledge gaps and research recommendations for essential tremor.

3. Climbing fiber-Purkinje cell synaptic pathology across essential tremor subtypes.

4. A step toward essential tremor gene discovery: identification of extreme phenotype and screening of HTRA2 and ANO3.

5. Mutation Analysis of HTRA2 Gene in Chinese Familial Essential Tremor and Familial Parkinson's Disease.

Review 6. Genomic Markers for Essential Tremor.