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Neurogenetics

Citations 181-190 of 574 total displayed.

Past content (since May 1998):

Original Contributions
Hereditary Spastic Paraplegia 3A Associated With Axonal Neuropathy
Neviana Ivanova; Kristl G. Claeys; Tine Deconinck; Ivan Litvinenko; Albena Jordanova; Michaela Auer-Grumbach; Jana Haberlova; Ann Löfgren; Gisele Smeyers; Eva Nelis; Rudy Mercelis; Barbara Plecko; Josef Priller; Josef Zámecník; Berten Ceulemans; Anne Kjersti Erichsen; Erik Björck; Garth Nicholson; Michael W. Sereda; Pavel Seeman; Ivo Kremensky; Vanio Mitev; Peter De Jonghe
Arch Neurol 2007; 64: 706-713. [Abstract] [Full text] [PDF]  

Observations
Vasculitic Neuropathy in a Patient With Hereditary C1 Inhibitor Deficiency
Yusuke Yakushiji; Haruo Mizuta; Kazuhiro Kurohara; Hiroyuki Onoue; Ryuichiro Okada; Toshiro Yoshimura; Yasuo Kuroda
Arch Neurol 2007; 64: 731-733. [Abstract] [Full text] [PDF]  

Observations
Association of a Presenilin 1 S170F Mutation With a Novel Alzheimer Disease Molecular Phenotype
Alessandra Piccini; Gianluigi Zanusso; Roberta Borghi; Cristiana Noviello; Salvatore Monaco; Roberta Russo; Gianluca Damonte; Andrea Armirotti; Matteo Gelati; Renzo Giordano; Pamela Zambenedetti; Claudio Russo; Bernardino Ghetti; Massimo Tabaton
Arch Neurol 2007; 64: 738-745. [Abstract] [Full text] [PDF]  

Observations
A New Episodic Ataxia Syndrome With Linkage to Chromosome 19q13
Kevin A. Kerber; Joanna C. Jen; Hane Lee; Stanley F. Nelson; Robert W. Baloh
Arch Neurol 2007; 64: 749-752. [Abstract] [Full text] [PDF]  

Editorials
Measuring the Risk of Alzheimer Disease
Roger N. Rosenberg
Arch Neurol 2007; 64: 479-480. [Extract] [Full text] [PDF]  

Original Contributions
The Association Between Genetic Variants in SORL1 and Alzheimer Disease in an Urban, Multiethnic, Community-Based Cohort
Joseph H. Lee; Rong Cheng; Nicole Schupf; Jennifer Manly; Rafael Lantigua; Yaakov Stern; Ekaterina Rogaeva; Yosuke Wakutani; Lindsay Farrer; Peter St. George-Hyslop; Richard Mayeux
Arch Neurol 2007; 64: 501-506. [Abstract] [Full text] [PDF]  

Original Contributions
Multiplex Families With Multiple System Atrophy
Kenju Hara; Yoshio Momose; Susumu Tokiguchi; Mitsuteru Shimohata; Kenshi Terajima; Osamu Onodera; Akiyoshi Kakita; Mitsunori Yamada; Hitoshi Takahashi; Motoyuki Hirasawa; Yoshikuni Mizuno; Katsuhisa Ogata; Jun Goto; Ichiro Kanazawa; Masatoyo Nishizawa; Shoji Tsuji
Arch Neurol 2007; 64: 545-551. [Abstract] [Full text] [PDF]  

Original Contributions
Mutation of the Linker Region of the Polymerase {gamma}-1 (POLG1) Gene Associated With Progressive External Ophthalmoplegia and Parkinsonism
Gavin Hudson; Andrew M. Schaefer; Robert W. Taylor; Watcharee Tiangyou; Andrew Gibson; Graham Venables; Philip Griffiths; David J. Burn; Douglass M. Turnbull; Patrick F. Chinnery
Arch Neurol 2007; 64: 553-557. [Abstract] [Full text] [PDF]  

Observations
Reduced Penetrance in a Brazilian Family With Spinocerebellar Ataxia Type 10
Salmo Raskin; Tetsuo Ashizawa; Hélio A. G. Teive; Walter O. Arruda; Ping Fang; Rui Gao; Misti C. White; Lineu C. Werneck; Benjamin Roa
Arch Neurol 2007; 64: 591-594. [Abstract] [Full text] [PDF]  

Original Contributions
Genotype and Protein Expression After Bone Marrow Transplantation for Adrenoleukodystrophy
Stefan Schönberger; Peter Roerig; Dominik T. Schneider; Guido Reifenberger; Ulrich Göbel; Jutta Gärtner
Arch Neurol 64.5.noc60105. [Abstract] [Full text] []  

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