Brent Fogel: search on Z-Library

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1

Emerging therapies in Friedreich's ataxia

Aranca, Tanya V, Jones, Tracy M, Shaw, Jessica D, Staffetti, Joseph S, Ashizawa, Tetsuo, Kuo, Sheng-Han, Fogel, Brent L, Wilmot, George R, Perlman, Susan L, Onyike, Chiadi U, Ying, Sarah H, Zesiewicz,

Journal:

Neurodegenerative Disease Management

Year:

2016

Language:

english

File:

PDF, 1.03 MB

english, 2016

2

An approach to the patient with late-onset cerebellar ataxia

Fogel, Brent L, Perlman, Susan

Journal:

Nature Clinical Practice Neurology

Year:

2006

Language:

english

File:

PDF, 185 KB

english, 2006

3

Emotional detachment, gait ataxia, and cerebellar dysconnectivity associated with compound heterozygous mutations in the SPG7 gene

Ringman, John M., Qiao, Yuchuan, Garbin, Alexander, Fisher, Beth E., Fogel, Brent, Watari Knoell, Kecia, Chui, Helena C., Shi, Yonggang, Rexach, Jessica E.

Journal:

Year:

2020

File:

PDF, 1.22 MB

2020

4

Creutzfeldt–Jakob disease presenting with alien limb sign

Brent Fogel, Mark Wu, Sarah Kremen, Kolar Murthy, George Jackson, Zeba Vanek

Journal:

Movement Disorders

Year:

2006

Language:

english

File:

PDF, 128 KB

english, 2006

5

Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia

Brent L. Fogel, Ji Yong Lee, Jessica Lane, Amanda Wahnich, Sandy Chan, Alden Huang, Greg E. Osborn, Eric Klein, Catherine Mamah, Susan Perlman, Daniel H. Geschwind, Giovanni Coppola

Journal:

Movement Disorders

Year:

2012

Language:

english

File:

PDF, 844 KB

english, 2012

6

A family with combined mutations of the hemophilia A and X-linked adrenoleukodystrophy genes

Brent L. Fogel, Pari Young, Arthur R. Thompson, Susan Perlman

Journal:

Year:

2008

Language:

english

File:

PDF, 127 KB

english, 2008

7

Aberrant Splicing of the Senataxin Gene in a Patient with Ataxia with Oculomotor Apraxia Type 2

Brent L. Fogel, Ji Yong Lee, Susan Perlman

Journal:

Year:

2009

Language:

english

File:

PDF, 322 KB

english, 2009

8

Candidate Screening of theTRPC3Gene in Cerebellar Ataxia

Esther B. E. Becker, Brent L. Fogel, Sanjeev Rajakulendran, Anna Dulneva, Michael G. Hanna, Susan L. Perlman, Daniel H. Geschwind, Kay E. Davies

Journal:

Year:

2011

Language:

english

File:

PDF, 96 KB

english, 2011

9

Clinical features and molecular genetics of autosomal recessive cerebellar ataxias

Brent L Fogel, Susan Perlman

Journal:

The Lancet Neurology

Year:

2007

Language:

english

File:

PDF, 404 KB

english, 2007

10

Progressive spinocerebellar ataxia mimicked by a presumptive cerebellar arteriovenous malformation

Brent L. Fogel, Noriko Salamon, Susan Perlman

Journal:

European Journal of Radiology Extra

Year:

2009

Language:

english

File:

PDF, 409 KB

english, 2009

11

C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia

Fogel, Brent L., Pribadi, Mochtar, Pi, Sarah, Perlman, Susan L., Geschwind, Daniel H., Coppola, Giovanni

Journal:

Movement Disorders

Year:

2012

Language:

english

File:

PDF, 78 KB

english, 2012

12

A Family with Spinocerebellar Ataxia Type 5 Found to Have a Novel Missense Mutation within aSPTBN2Spectrin Repeat

Cho, Ellen, Fogel, Brent L.

Journal:

Year:

2013

Language:

english

File:

PDF, 201 KB

english, 2013

13

Mutations inPDYNare not responsible for multiple system atrophy

Brent L. Fogel, Cameron Baker, Andrew Curnow, Susan L. Perlman…

Journal:

Journal of Neurology

Year:

2013

Language:

english

File:

PDF, 155 KB

english, 2013

14

Clinical Neurogenetics

Shakkottai, Vikram G., Fogel, Brent L.

Journal:

Neurologic Clinics

Year:

2013

Language:

english

File:

PDF, 693 KB

english, 2013

15

Preface

Fogel, Brent L.

Journal:

Neurologic Clinics

Year:

2013

Language:

english

File:

PDF, 70 KB

english, 2013

16

Utilization of Genetic Testing Prior to Subspecialist Referral for Cerebellar Ataxia

Fogel, Brent L., Vickrey, Barbara G., Walton-Wetzel, Jenny, Lieber, Eli, Browner, Carole H.

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2013

Language:

english

File:

PDF, 139 KB

english, 2013

17

Exome Sequencing in the Clinical Diagnosis of Sporadic or Familial Cerebellar Ataxia

Fogel, Brent L., Lee, Hane, Deignan, Joshua L., Strom, Samuel P., Kantarci, Sibel, Wang, Xizhe, Quintero-Rivera, Fabiola, Vilain, Eric, Grody, Wayne W., Perlman, Susan, Geschwind, Daniel H., Nelson, S

Journal:

Year:

2014

Language:

english

File:

PDF, 521 KB

english, 2014

18

Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders

Lee, Hane, Deignan, Joshua L., Dorrani, Naghmeh, Strom, Samuel P., Kantarci, Sibel, Quintero-Rivera, Fabiola, Das, Kingshuk, Toy, Traci, Harry, Bret, Yourshaw, Michael, Fox, Michelle, Fogel, Brent L.,

Journal:

JAMA The Journal of the American Medical Association

Year:

2014

Language:

english

File:

PDF, 255 KB

english, 2014

19

The Neurogenetics of Atypical Parkinsonian Disorders

Fogel, Brent, Clark, Mary, Geschwind, Daniel

Journal:

Seminars in Neurology

Year:

2014

Language:

english

File:

PDF, 254 KB

english, 2014

20

A new model to study neurodegeneration in Ataxia Oculomotor Apraxia Type 2

Becherel, Olivier J., Sun, Jane, Yeo, Abrey J., Nayler, Sam, Fogel, Brent L., Gao, Fuying, Coppola, Giovanni, Criscuolo, Chiara, De Michele, Giuseppe, Wolvetang, Ernst, Lavin, Martin F.

Journal:

Human Molecular Genetics

Year:

2015

Language:

english

File:

PDF, 1.43 MB

english, 2015

21

New-Onset Psychosis in a Patient With Spinocerebellar Ataxia Type 10

Wexler, Eric, Fogel, Brent L.

Journal:

American Journal of Psychiatry

Year:

2011

Language:

english

File:

PDF, 229 KB

english, 2011

22

ELAVL2-regulated transcriptional and splicing networks in human neurons link neurodevelopment and autism

Berto, Stefano, Usui, Noriyoshi, Konopka, Genevieve, Fogel, Brent L.

Journal:

Human Molecular Genetics

Year:

2016

Language:

english

File:

PDF, 1.19 MB

english, 2016

23

Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?

Fogel, Brent L., Hanson, Sonya M., Becker, Esther B. E.

Journal:

Movement Disorders

Year:

2015

Language:

english

File:

PDF, 4.35 MB

english, 2015

24

Clinical exome sequencing in neurogenetic and neuropsychiatric disorders

Fogel, Brent L., Lee, Hane, Strom, Samuel P., Deignan, Joshua L., Nelson, Stanley F.

Journal:

Annals of the New York Academy of Sciences

Year:

2016

Language:

english

File:

PDF, 653 KB

english, 2016

25

Magnetic Resonance Imaging Abnormalities in the Corpus Callosum of a Patient With Neuropsychiatric Lupus

Fogel, Brent, Cardenas, Doris, Ovbiagele, Bruce

Journal:

The Neurologist

Year:

2006

Language:

english

File:

PDF, 223 KB

english, 2006

26

Interpretation of Genetic Testing

Fogel, Brent L.

Journal:

CONTINUUM: Lifelong Learning in Neurology

Year:

2011

Language:

english

File:

PDF, 138 KB

english, 2011

27

The need to develop a patient-centered precision medicine model for adults with chronic disability

Wolf, Susan M., Thyagarajan, Bharat, Fogel, Brent L.

Journal:

Expert Review of Molecular Diagnostics

Year:

2017

Language:

english

File:

PDF, 590 KB

english, 2017

28

[Handbook of Clinical Neurology] Neurogenetics, Part I Volume 147 || Autosomal-recessive cerebellar ataxias

Fogel, Brent L.

Year:

2018

Language:

english

File:

PDF, 876 KB

english, 2018

29

[Handbook of Clinical Neurology] Neurogenetics, Part I Volume 147 || Genetic and genomic testing for neurologic disease in clinical practice

Fogel, Brent L.

Year:

2018

Language:

english

File:

PDF, 298 KB

english, 2018

30

Collaborative Science Unites Researchers and a Novel Spastic Ataxia Gene

Fogel, Brent L.

Journal:

Annals of Neurology

Year:

2018

Language:

english

File:

PDF, 610 KB

english, 2018

31

Successful treatment of a genetic childhood ataxia due to riboflavin transporter deficiency

Fan, Judy, Fogel, Brent L.

Journal:

Cerebellum & Ataxias

Year:

2018

Language:

english

File:

PDF, 495 KB

english, 2018

32

A family with spinocerebellar ataxia and retinitis pigmentosa attributed to an ELOVL4 mutation

Xiao, Changrui, M. Binkley, Elaine, Rexach, Jessica, Knight-Johnson, Amy, Khemani, Pravin, Fogel, Brent L., Das, Soma, M. Stone, Edwin, Gomez, Christopher M.

Journal:

Neurology: Genetics

Year:

2019

File:

PDF, 816 KB

2019

33

P4-182: NEURONAL AND OLIGODENDROGLIAL EXOSOMAL Î±-SYNUCLEIN DISTINGUISHES PARKINSON'S DISEASE FROM MULTIPLE SYSTEM ATROPHY

Dutta, Suman, del Rosario, Irish, Paul, Kimberly, Palma, Jose Alberto, Perlman, Susan L., Poon, Wayne W., Kaufmann, Horacio, Fogel, Brent L., Bronstein, Jeff M., Ritz, Beate, Bitan, Gal

Journal:

Alzheimer's & Dementia

Year:

2019

File:

PDF, 109 KB

2019

34

The Neurodevelopmental and Motor Phenotype of SCA21 (ATX-TMEM240)

Burdekin, Emma D., Fogel, Brent L., Jeste, Shafali S., Martinez, Julian, Rexach, Jessica E., DiStefano, Charlotte, Hyde, Carly, Safari, Tabitha, Wilson, Rujuta B.

Journal:

Journal of Child Neurology

Year:

2020

File:

PDF, 235 KB

2020