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1

Botulinum Toxin Injection Techniques for the Management of Adult Spasticity

Walker, Heather W., Lee, Michael Y., Bahroo, Laxman B., Hedera, Peter, Charles, David

Journal:

Year:

2015

Language:

english

File:

PDF, 562 KB

english, 2015

2

Diagnosis and Treatment of Wilson's Disease

Brewer, George, Fink, John, Hedera, Peter

Journal:

Seminars in Neurology

Year:

1999

Language:

english

File:

PDF, 1.03 MB

english, 1999

3

Autosomal recessive primary generalized dystonia in two siblings from a consanguineous family

Paolo Moretti, Peter Hedera, John Wald, John Fink

Journal:

Movement Disorders

Year:

2005

Language:

english

File:

PDF, 53 KB

english, 2005

4

Positive family history of essential tremor influences the motor phenotype of Parkinson's disease

Peter Hedera, John Y. Fang, Fenna Phibbs, Michael K. Cooper, P. David Charles, Thomas L. Davis

Journal:

Movement Disorders

Year:

2009

Language:

english

File:

PDF, 176 KB

english, 2009

5

Familial genetic predisposition, epilepsy localization and antecedent febrile seizures

B. Abou-Khalil, L. Krei, B. Lazenby, P.A. Harris, J.L. Haines, P. Hedera

Journal:

Epilepsy Research

Year:

2007

Language:

english

File:

PDF, 198 KB

english, 2007

6

Myelopolyneuropathy and pancytopenia due to copper deficiency and high zinc levels of unknown origin II. The denture cream is a primary source of excessive zinc

Peter Hedera, Amanda Peltier, John K. Fink, Sandy Wilcock, Zachary London, George J. Brewer

Journal:

NeuroToxicology

Year:

2009

Language:

english

File:

PDF, 101 KB

english, 2009

7

New Ideas in Epilepsy Genetics

Gurnett, Christina A., Hedera, Peter

Journal:

Archives of Neurology

Year:

2007

Language:

english

File:

PDF, 126 KB

english, 2007

8

Reversible Dementia

Clarfield, A. M., Friedland, R. P., Hedera, P.

Journal:

Year:

1995

Language:

english

File:

PDF, 196 KB

english, 1995

9

Hereditary Spastic Paraplegia: Genetic Heterogeneity and Genotype-Phenotype Correlation

Fink, John, Hedera, Peter

Journal:

Seminars in Neurology

Year:

1999

File:

PDF, 929 KB

1999

10

Diagnosis and Treatment of Wilson's Disease

Brewer, George, Fink, John, Hedera, Peter

Journal:

Seminars in Neurology

Year:

1999

File:

PDF, 1.03 MB

1999

11

Hereditary Spastic Paraplegia: Genetic Heterogeneity and Genotype-Phenotype Correlation

Fink, John, Hedera, Peter

Journal:

Seminars in Neurology

Year:

1999

Language:

english

File:

PDF, 929 KB

english, 1999

12

Deep brain stimulation may reduce the relative risk of clinically important worsening in early stage Parkinson's disease

Hacker, Mallory L., Tonascia, James, Turchan, Maxim, Currie, Amanda, Heusinkveld, Lauren, Konrad, Peter E., Davis, Thomas L., Neimat, Joseph S., Phibbs, Fenna T., Hedera, Peter, Wang, Lily, Shi, Yapin

Journal:

Parkinsonism & Related Disorders

Year:

2015

Language:

english

File:

PDF, 746 KB

english, 2015

13

Cortical Implications of Advancing Age and Disease Duration in Parkinson’s Disease Patients with Postural Instability and Gait Dysfunction

Herb, Joshua N., Rane, Swati, Isaacs, David A., Van Wouwe, Nelleke, Roman, Olivia C., Landman, Bennett A., Dawant, Benoit M., Hedera, Peter, Zald, David H., Neimat, Joseph S., Wylie, Scott A., Donahue

Journal:

Journal of Parkinson s Disease

Year:

2016

Language:

english

File:

PDF, 1.25 MB

english, 2016

14

Wilson's disease: A master of disguise

Journal:

Parkinsonism & Related Disorders

Year:

2019

Language:

english

File:

PDF, 694 KB

english, 2019

15

Prenatal diagnosis of hereditary spastic paraplegia

Peter Hedera, Jeffrey A. Williamson, Shirley Rainier, David Alvarado, Turgut Tukel, Memnune Apak, John K. Fink

Journal:

Prenatal Diagnosis

Year:

2001

Language:

english

File:

PDF, 78 KB

english, 2001

16

Possible third case of Lin-Gettig syndrome

Peter Hedera, Jeffrey W. Innis

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 101 KB

english, 2002

17

Retinitis pigmentosa, growth hormone deficiency, and acromelic skeletal dysplasia in two brothers: Possible familial RHYNS syndrome

Peter Hedera, Jerome L. Gorski

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 125 KB

english, 2001

18

Juberg–Hayward syndrome: Report of a new patient with severe phenotype and novel clinical features

Peter Hedera, Jeffrey W. Innis

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 106 KB

english, 2003

19

Oculo-facio-cardio-dental syndrome: Skewed X chromosome inactivation in mother and daughter suggest X-linked dominant Inheritance

Peter Hedera, Jerome L. Gorski

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 158 KB

english, 2003

20

Two patients with monomelic ulnar duplication with mirror hand polydactyly: Segmental Laurin–Sandrow syndrome

Jeffrey W. Innis, Peter Hedera

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 146 KB

english, 2004

21

Skewed X-inactivation in carriers establishes linkage in an X-linked deafness–mental retardation syndrome

Frank J. Probst, Peter Hedera, Anthony M. Sclafani, Maria Grazia Pomponi, Giovanni Neri, Jessica Tyson, Julie A. Douglas, Elizabeth M. Petty, Donna M. Martin

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 68 KB

english, 2004

22

Skewed X-inactivation in carriers establishes linkage in an X-linked deafness-mental retardation syndrome (Am J Med Genet 131A: 209–212)

Frank J. Probst, Peter Hedera, Anthony M. Sclafani, Maria Grazia Pomponi, Giovanni Neri, Jessica Tyson, Julie A. Douglas, Elizabeth M. Petty, Donna M. Martin

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 26 KB

english, 2005

23

Novel mental retardation–epilepsy syndrome linked to Xp21.1–p11.4

Peter Hedera, David Alvarado, Ahmad Beydoun, John K. Fink

Journal:

Annals of Neurology

Year:

2002

Language:

english

File:

PDF, 109 KB

english, 2002

24

Treatment of Wilson's disease with zinc. XVII: Treatment during pregnancy

George J. Brewer, Virginia D. Johnson, Robert D. Dick, Peter Hedera, John K. Fink, Karen J. Kluin

Journal:

Year:

2000

Language:

english

File:

PDF, 76 KB

english, 2000

25

Assessment of cerebral blood flow reserve using functional magnetic resonance imaging

Peter Hedera, Song Lai, Jonathan S. Lewin, E. Mark Haacke, Dee Wu, Alan J. Lerner, Robert P. Friedland

Journal:

Journal of Magnetic Resonance Imaging

Year:

1996

Language:

english

File:

PDF, 963 KB

english, 1996

26

Familial essential tremor with apparent autosomal dominant inheritance: Should we also consider other inheritance modes?

Shaochun Ma, Thomas L. Davis, Marcia A. Blair, John Y. Fang, Yuki Bradford, Jonathan L. Haines, Peter Hedera

Journal:

Movement Disorders

Year:

2006

Language:

english

File:

PDF, 109 KB

english, 2006

27

Prevalence of unilateral tremor in autosomal dominant essential tremor

Fenna Phibbs, John Y. Fang, Michael K. Cooper, David P. Charles, Thomas L. Davis, Peter Hedera

Journal:

Movement Disorders

Year:

2009

Language:

english

File:

PDF, 438 KB

english, 2009

28

Identification of vascular structures as a major source of signal contrast in high resolution 2D and 3D functional activation imaging of the motor cortex at l.5T preliminary results

S. Lai, A. L. Hopkins, E. M. Haacke, D. Li, B. A. Wasserman, P. Buckley, L. Friedman, H. Meltzer, P. Hedera, R. Friedland

Journal:

Magnetic Resonance in Medicine

Year:

1993

Language:

english

File:

PDF, 784 KB

english, 1993

29

2D and 3D high resolution gradient echo functional imaging of the brain: Venous contributions to signal in motor cortex studies

E. M. Haacke, A. Hopkins, S. Lai, P. Buckley, L. Friedman, H. Meltzer, P. Hedera, R. Friedland, S. Klein, L. Thompson, D. Detterman, J. Tkach, J. S. Lewin

Journal:

NMR in Biomedicine

Year:

1994

Language:

english

File:

PDF, 3.07 MB

english, 1994

30

Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy

Shaochun Ma, Marcia A. Blair, Bassel Abou-Khalil, Andre H. Lagrange, Christina A. Gurnett, Peter Hedera

Journal:

Epilepsy Research

Year:

2006

Language:

english

File:

PDF, 172 KB

english, 2006

31

High-throughput mutational analysis ofTOR1Ain primary dystonia

Jianfeng Xiao, Robert W Bastian, Joel S Perlmutter, Brad A Racette, Samer D Tabbal, Morvarid Karimi, Randal C Paniello, Andrew Blitzer, Dev Sat Batish, Zbigniew K Wszolek, Ryan J Uitti, Peter Hedera,

Journal:

BMC Medical Genetics

Year:

2009

Language:

english

File:

PDF, 1.34 MB

english, 2009

32

The GABBR1 locus and the G1465A variant is not associated with temporal lobe epilepsy preceded by febrile seizures

Shaochun Ma, Bassel Abou-Khalil, James S Sutcliffe, Jonathan L Haines, Peter Hedera

Journal:

BMC Medical Genetics

Year:

2005

Language:

english

File:

PDF, 478 KB

english, 2005

33

Addition of individual chromosomes of maize inbreds B73 and Mo17 to oat cultivars Starter and Sun II: maize chromosome retention, transmission, and plant phenotype

Howard W. Rines, Ronald L. Phillips, Ralf G. Kynast, Ron J. Okagaki, Mark W. Galatowitsch, Paul A. Huettl, Adrian O. Stec, Morrison S. Jacobs, Jayanti Suresh, Hedera L. Porter, Matthew D. Walch, Candi

Journal:

Theoretical and Applied Genetics

Year:

2009

Language:

english

File:

PDF, 472 KB

english, 2009

34

Spinal cord magnetic resonance imaging in autosomal dominant hereditary spastic paraplegia

P. Hedera, O. P. Eldevik, P. Maly, S. Rainier, J. K. Fink

Journal:

Year:

2005

Language:

english

File:

PDF, 234 KB

english, 2005

35

Mutation inKIF5Acan also cause adult-onset hereditary spastic paraplegia

Marcia A. Blair, Shaochun Ma, Peter Hedera

Journal:

Year:

2006

Language:

english

File:

PDF, 130 KB

english, 2006

36

Autosomal Dominant Lateral Temporal Epilepsy: Two Families with Novel Mutations in the LGI1 Gene

Peter Hedera, Bassel Abou-Khalil, Amy E. Crunk, Kelly A. Taylor, Jonathan L. Haines, James S. Sutcliffe

Journal:

Year:

2004

Language:

english

File:

PDF, 127 KB

english, 2004

37

Genetic variants in the IMPA2 gene do not confer increased risk of febrile seizures in Caucasian patients

M. A. Blair, S. Ma, B. Abou-Khalil, P. Hedera

Journal:

European Journal of Neurology

Year:

2007

Language:

english

File:

PDF, 460 KB

english, 2007

38

Hereditary spastic paraplegia or spinocerebellar ataxia? Not always as easy as it seems

Journal:

European Journal of Neurology

Year:

2009

Language:

english

File:

PDF, 57 KB

english, 2009

39

Identification of a Novel Locus for Febrile Seizures and Epilepsy on Chromosome 21q22

Peter Hedera, Shaochun Ma, Marcia A. Blair, Kelly A. Taylor, Aline Hamati, Yuki Bradford, Bassel Abou-Khalil, Jonathan L. Haines

Journal:

Year:

2006

Language:

english

File:

PDF, 226 KB

english, 2006

40

A new locus for autosomal dominant generalized epilepsy associated with mild mental retardation on chromosome 3p

Marcia A. Blair, Bassel Abou-Khalil, Amy Crunk, Jonathan L. Haines, Peter Hedera

Journal:

Year:

2011

Language:

english

File:

PDF, 443 KB

english, 2011

41

Stroke risk factors and development of collateral flow in carotid occlusive disease

P. Hedera, J. Bujdáková, P. Traubner, J. Pancák

Journal:

Acta Neurologica Scandinavica

Year:

1998

Language:

english

File:

PDF, 520 KB

english, 1998

42

Amyloid-β Protein Angiopathies Masquerading as Alzheimer's Disease?

D. L. COHEN, P. HEDERA, D. R. D. PREMKUMAR, R. P. FRIEDLAND, R. N. KALARIA

Journal:

Annals of the New York Academy of Sciences

Year:

1997

Language:

english

File:

PDF, 371 KB

english, 1997

43

Neuroimaging of Vessel Amyloid in Alzheimer's Disease

ROBERT P. FRIEDLAND, RAJESH KALARIA, MARC BERRIDGE, FLORO MIRALDI, PETER HEDERA, JOHN RENO, LEON LYLE, CHARLES A. MAROTTA

Journal:

Annals of the New York Academy of Sciences

Year:

1997

Language:

english

File:

PDF, 381 KB

english, 1997

44

10.1038/ng758

Zhao, Xinping, Alvarado, David, Rainier, Shirley, Lemons, Rosemary, Hedera, Peter, Weber, Christian H., Tukel, Turgut, Apak, Memnune, Heiman-Patterson, Terry, Ming, Lei, Bui, Melanie, Fink, John K.

Journal:

Nature Genetics

Year:

2001

Language:

english

File:

PDF, 2.37 MB

english, 2001

45

Blood flow velocities in basilar artery during rotation of the head

P. Hedera, J. Bujdáková, P. Traubner

Journal:

Acta Neurologica Scandinavica

Year:

1993

Language:

english

File:

PDF, 561 KB

english, 1993

46

Clustering of dystonia in some pedigrees with autosomal dominant essential tremor suggests the existence of a distinct subtype of essential tremor

Peter Hedera, Fenna T Phibbs, John Y Fang, Michael K Cooper, P David Charles, Thomas L Davis

Journal:

Year:

2010

Language:

english

File:

PDF, 885 KB

english, 2010

47

Maternal intrachromosomal insertional translocation leads to recurrent 1q21.3q23.3 deletion in two siblings

Shane C. Quinonez, Peter Hedera, Mason Barr, Todd Ackley, Cindy Lam, Anjali Purkayastha, Thomas W. Glover, Jeffrey W. Innis

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 265 KB

english, 2012

48

The effect of HSP-causing mutations in SPG3A and NIPA1 on the assembly, trafficking, and interaction between atlastin-1 and NIPA1

Emmanuel J. Botzolakis, Jiali Zhao, Katharine N. Gurba, Robert L. Macdonald, Peter Hedera

Journal:

Molecular and Cellular Neuroscience

Year:

2011

Language:

english

File:

PDF, 2.64 MB

english, 2011

49

Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizures

Shaochun Ma, Bassel Abou-Khalil, Marcia A. Blair, James S. Sutcliffe, Jonathan L. Haines, Peter Hedera

Journal:

Neuroscience Letters

Year:

2006

Language:

english

File:

PDF, 90 KB

english, 2006

50

G.O.5 A new autosomal dominant distal vacuolar myopathy associated with mutation of the nuclear matrix protein, matrin 3

J. Senderek, S.M. Garvey, M. Krieger, I. Tournev, M. Elbracht, A. Roos, C. Stendel, A. Urtizberea, V. Guergueltcheva, V. Mihailova, H. Feit, J. Tramonte, P. Hedera, C. Bergmann, S. Rudnik-Schöneborn,

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 43 KB

english, 2009