B. Kremer

发表

Postural responses to multidirectional stance perturbations in cerebellar ataxia

J. Allum, B. Bloem, B. P. Warrenburg, 2006, Experimental Neurology.

Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm

M. Hayden, B. Kremer, S. Andrew, 1994, Nature Genetics.

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

M. Hayden, B. Kremer, F. Squitieri, 1993, Nature Genetics.

Apathy Is Not Depression in Huntington ’ s Disease

P. Eling, B. Kremer, P. Naarding, 2009 .

Trunk sway in patients with spinocerebellar ataxia

Bastiaan R Bloem, J. Allum, B. Bloem, 2005, Movement disorders : official journal of the Movement Disorder Society.

Aripiprazole in the treatment of Alzheimer's disease

P. D. De Deyn, B. Kremer, R. O. Oude Voshaar, 2013, Expert opinion on pharmacotherapy.

Cerebrospinal fluid amyloid beta42/phosphorylated tau ratio discriminates between Alzheimer's disease and vascular dementia.

M. Verbeek, B. Kremer, R. Jansen, 2006, The journals of gerontology. Series A, Biological sciences and medical sciences.

Scale for the assessment and rating of ataxia

L. Baliko, C. Globas, A. Durr, 2006, Neurology.

ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia

J. Cruysberg, J. Timmermans, H. J. Schelhaas, 2008, neurogenetics.

Inhibition of amyloid-β-induced cell death in human brain pericytes in vitro

M. Verbeek, B. Kremer, H. J. Donkelaar, 2002, Brain Research.

Falls in degenerative cerebellar ataxias

Bart P C van de Warrenburg, Bastiaan R Bloem, Marten Munneke, 2005, Movement disorders : official journal of the Movement Disorder Society.

Prior Anticoagulant Therapy, Subtherapeutic International Normalized Ratio and Thrombolytic Therapy in Acute Ischemic Stroke

B. Kremer, J. De Keyser, G. Luijckx, 2011, International journal of stroke : official journal of the International Stroke Society.

Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23.

C. Wijmenga, R. Sinke, R. Zubarev, 2010, American journal of human genetics.

ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia

J. Cruysberg, J. Timmermans, H. J. Schelhaas, 2008, neurogenetics.

Creatine protects against 3-nitropropionic acid-induced cell death in murine corticostriatal slice cultures

M. Verbeek, B. Kremer, R. Waal, 2004, Brain Research.

3-Nitropropionic acid induces cell death and mitochondrial dysfunction in rat corticostriatal slice cultures

M. Verbeek, B. Kremer, R. Waal, 2002, Neuroscience Letters.

Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia

Cleo C. van Diemen, C. Wijmenga, R. Sinke, 2017, Brain : a journal of neurology.

Imminent brain death: point of departure for potential heart-beating organ donor recognition

A. Maas, M. Kuiper, E. Wijdicks, 2010, Intensive Care Medicine.

Attitudes toward direct predictive testing for the Huntington disease gene. Relevance for other adult-onset disorders. The Canadian Collaborative Group on Predictive Testing for Huntington Disease.

M. Hayden, B. Kremer, J. Theilmann, 1993, JAMA.

AMPA and NMDA binding sites in the hypothalamic lateral tuberal nucleus

R. Albin, S. Tallaksen-Greene, B. Kremer, 1993, Neurology.

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.

Enrico Amico, Philippe Allain, Mark Mühlau, 2017, The Lancet. Neurology.

DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence.

I. Kanazawa, M. Hayden, B. Kremer, 1994, Human molecular genetics.

Intrastriatal gradient analyses of 18F-FDOPA PET scans for differentiation of Parkinsonian disorders

K. Leenders, B. Kremer, D. Vállez García, 2020, NeuroImage: Clinical.

Cerebrospinal fluid tau levels in frontotemporal dementia

P. Scheltens, Y. Pijnenburg, M. Verbeek, 2005, Annals of neurology.

Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19

C. Wijmenga, M. Swertz, R. Sinke, 2012, Annals of neurology.

Apathy Is Not Depression in Huntington’s Disease

P. Eling, B. Kremer, P. Naarding, 2009 .

Imaging of neuroinflammation due to repetitive head injury in currently active kickboxers

B. Kremer, R. Renken, J. Spikman, 2021, European Journal of Nuclear Medicine and Molecular Imaging.

SPG10 is a rare cause of spastic paraplegia in European families

R. Schüle, L. Schöls, J. Kassubek, 2008, Journal of Neurology, Neurosurgery, and Psychiatry.

University of Groningen Mutations in Potassium Channel KCND 3 Cause Spinocerebellar Ataxia Type 19

C. Wijmenga, M. Swertz, R. Sinke, 2012 .

P3-045 Tau protein phosphorylated at threonine 181 in cerebrospinal fluid as a possible biomarker for Alzheimer's disease

D. Jong, M. Verbeek, B. Kremer, 2004, Neurobiology of Aging.

Language impairment in cerebellar ataxia

B. P. Warrenburg, B. Kremer, S. Knuijt, 2014, Movement disorders : official journal of the Movement Disorder Society.

Inhibition of amyloid-beta-induced cell death in human brain pericytes in vitro.

M. Verbeek, B. Kremer, R. D. de Waal, 2002, Brain research.

Insulin inhibits amyloid beta-induced cell death in cultured human brain pericytes.

H. T. ten Donkelaar, M. Verbeek, B. Kremer, 2004, Neurobiology of aging.

Expression pattern of apoptosis-related markers in Huntington’s disease

P. Wesseling, M. Verbeek, B. Kremer, 2005, Acta Neuropathologica.

Neuropathology in classical and variant ataxia‐telangiectasia

B. Kremer, M. van Deuren, M. Willemsen, 2012, Neuropathology : official journal of the Japanese Society of Neuropathology.

Hereditary Late-Onset Chorea Without Significant Dementia

J. Britton, M. Hayden, R. Robinson, 1995, Neurology.

Normal CAG repeat length in the Huntington's disease gene in senile chorea

M. Hayden, B. Kremer, D. Calne, 1994, Neurology.

New Insights Into the Clinical Features, Pathogenesis and Molecular Genetics of Huntington Disease

M. Hayden, B. Kremer, B. Weber, 1992, Brain pathology.

Presence of ATM protein and residual kinase activity correlates with the phenotype in ataxia‐telangiectasia: A genotype–phenotype study

A. Broeks, N. Wulffraat, C. Catsman-Berrevoets, 2012, Human mutation.

Recent Advances in Hereditary Spinocerebellar Ataxias

R. Sinke, B. Kremer, B. V. D. van de Warrenburg, 2005, Journal of neuropathology and experimental neurology.

Autosomal recessive cerebellar ataxias: the current state of affairs

B. Kremer, H. Scheffer, N. Knoers, 2011, Journal of Medical Genetics.

Riluzole in Huntington's disease: a 3‐year, randomized controlled study

B. Dubois, H. Przuntek, A. Ludolph, 2007, Annals of neurology.

Influence of lamotrigine on progression of early Huntington disease

L. Raymond, M. Hayden, C. Jacova, 1999, Neurology.

PTPRR Protein Tyrosine Phosphatase Isoforms and Locomotion of Vesicles and Mice

B. Kremer, J. Fransen, W. Hendriks, 2009, The Cerebellum.

Diagnosis of Huntington disease: a model for the stages of psychological response based on experience of a predictive testing program.

M. Hayden, B. Kremer, J. Theilmann, 1993, American journal of medical genetics.

Spinocerebellar Ataxia Types 1, 2, 3 and 6: the Clinical Spectrum of Ataxia and Morphometric Brainstem and Cerebellar Findings

D. Timmann, P. Bauer, L. Schöls, 2012, The Cerebellum.

Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic cases.

M. Hayden, B. Kremer, F. Squitieri, 1993, Journal of medical genetics.

Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects

M. Hayden, B. Kremer, F. Squitieri, 1993, Nature genetics.

Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes.

M. Hayden, B. Kremer, Y. P. Goldberg, 1995, American journal of human genetics.

Spinocerebellar Ataxia Types 1, 2, 3 and 6: the Clinical Spectrum of Ataxia and Morphometric Brainstem and Cerebellar Findings

L. Baliko, C. Globas, D. Timmann, 2008, The Cerebellum.

A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats.

Paul W Goldberg, M. Hayden, P. Goldberg, 1994, The New England journal of medicine.

No evidence for decreased D2/3 receptor availability and frontal hypoperfusion in subjects with compulsive pornography use

R. Schoevers, B. Kremer, J. Booij, 2021, Psychiatry Research: Neuroimaging.

CSF neurofilament proteins levels are elevated in sporadic Creutzfeldt-Jakob disease.

W. F. Abdo, M. Verbeek, B. Kremer, 2010, Journal of Alzheimer's disease : JAD.

Hereditary late-onset chorea without significant dementia: Genetic evidence for substantial phenotypic variation in Huntington’s disease

M. Hayden, R. Robinson, B. Kremer, 2019 .

Huntington disease without CAG expansion: phenocopies or errors in assignment?

M. Hayden, G. Campanella, B. Kremer, 1994, American journal of human genetics.

Molecular analysis of late onset Huntington's disease.

M. Hayden, B. Kremer, F. Squitieri, 1993, Journal of medical genetics.

Responsiveness of different rating instruments in spinocerebellar ataxia patients

R. Fimmers, D. Timmann, T. Schmitz-Hübsch, 2010, Neurology.

Serum MHPG strongly predicts conversion to Alzheimer's disease in behaviorally characterized subjects with Down syndrome.

C. V. van Duijn, B. Kremer, P. Naudé, 2014, Journal of Alzheimer's disease : JAD.

[Embrace, a model for integrated elderly care].

R. Brans, B. Kremer, B. Middel, 2014, Tijdschrift voor gerontologie en geriatrie.

Embrace, a model for integrated elderly care: study protocol of a randomized controlled trial on the effectiveness regarding patient outcomes, service use, costs, and quality of care

B. Kremer, K. Wynia, S. Reijneveld, 2013, BMC Geriatrics.

Functional Analysis Helps to Define KCNC3 Mutational Spectrum in Dutch Ataxia Cases

R. Sinke, B. Kremer, E. Boddeke, 2015, PloS one.

Pathogenesis of cerebral amyloid angiopathy

M. Verbeek, B. Kremer, A. Rensink, 2003, Brain Research Reviews.

PIPS one No Effect of One-Year Treatment with Indomethacin on Alzheimer ' s Disease Progression : A Randomized Controlled Trial

W. Hoefnagels, G. Borm, M. Verbeek, 2017 .

No Effect of One-Year Treatment with Indomethacin on Alzheimer's Disease Progression: A Randomized Controlled Trial

W. Hoefnagels, G. Borm, M. Verbeek, 2008, PloS one.

Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxia.

A. Hoischen, N. Drouot, J. Veltman, 2010, American journal of human genetics.

The prevalence and severity of disease-related disabilities and their impact on quality of life in neuromuscular diseases

G. Drost, B. Kremer, J. Almansa, 2019, Disability and rehabilitation.

Scale for the Assessment and Rating of Ataxia (SARA)

A. Durr, L. Schöls, T. Schmitz-Hübsch, 2010 .

Attitudes Toward Direct Predictive Testing for the Huntington Disease Gene: Relevance for Other Adult-Onset Disorders

M. Hayden, W. Meschino, O. Suchowersky, 1993 .

Self‐rated health status in spinocerebellar ataxia—Results from a European multicenter study

Paola Giunti, Dagmar Timmann, Sylvia Boesch, 2010, Movement disorders : official journal of the Movement Disorder Society.

Recurrent major depression, ataxia, and cardiomyopathy: association with a novel POLG mutation?

W. Verhoeven, B. Kremer, C. Marcelis, 2011, Neuropsychiatric disease and treatment.

Peripheral nerve involvement in spinocerebellar ataxias.

N. van Alfen, M. Zwarts, R. Sinke, 2004, Archives of neurology.

Cerebral Autoregulation in Stroke

M. Aries, B. Kremer, J. Elting, 2010 .

“Ears of the Lynx” MRI Sign Is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia

N. Bresolin, J. Masdeu, M. Riverol, 2019, American Journal of Neuroradiology.

Neuropsychiatric Disease and Treatment Dovepress Recurrent Major Depression, Ataxia, and Cardiomyopathy: Association with a Novel Polg Mutation? Jos Im Egger Boudewijn Jhb De Pont

W. Verhoeven, B. Kremer, C. Marcelis, 2022 .

Cerebellar Cognitive Affective Syndrome and Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay: A Report of Two Male Sibs

W. Verhoeven, B. Kremer, S. Vermeer, 2012, Psychopathology.

Cerebrospinal fluid analysis differentiates multiple system atrophy from Parkinson's disease

W. F. Abdo, B. Bloem, M. Horstink, 2004, Movement disorders : official journal of the Movement Disorder Society.

Differential gene expression in human brain pericytes induced by amyloid‐β protein

M. Verbeek, B. Kremer, R. D. de Waal, 2004, Neuropathology and applied neurobiology.

Insulin inhibits amyloid β-induced cell death in cultured human brain pericytes

M. Verbeek, B. Kremer, H. J. Donkelaar, 2004, Neurobiology of Aging.

Expression of the cytokine leukemia inhibitory factor and pro-apoptotic insulin-like growth factor binding protein-3 in Alzheimer's disease

Irene Otte-Höller, Marcel M. Verbeek, Hans J. ten Donkelaar, 2002, Acta Neuropathologica.

POTENTIAL PITFALLS IN THE ANALYSIS OF CSF BIOMARKERS IN ALZHEIMER'S DISEASE AND VASCULAR DEMENTIA

D. Jong, M. Verbeek, B. Kremer, 2007 .

Authors’ Response POTENTIAL PITFALLS IN THE ANALYSIS OF CSF BIOMARKERS IN ALZHEIMER’S DISEASE AND VASCULAR DEMENTIA

D. Jong, M. Verbeek, B. Kremer, 2007 .

Reliability and validity of the International Cooperative Ataxia Rating Scale: A study in 156 spinocerebellar ataxia patients

Paola Giunti, Bart P C van de Warrenburg, Sylvia Boesch, 2006, Movement disorders : official journal of the Movement Disorder Society.

Age at onset variance analysis in spinocerebellar ataxias: A study in a Dutch–French cohort

H. Hendriks, R. Sinke, A. Dürr, 2005, Annals of neurology.

SCA Functional Index

D. Timmann, T. Schmitz-Hübsch, T. Klockgether, 2008, Neurology.

The cerebrospinal fluid amyloid beta42/40 ratio in the differentiation of Alzheimer's disease from non-Alzheimer's dementia.

F. Verhey, M. Verbeek, B. Kremer, 2010, Current Alzheimer research.

Monoamines and their metabolites in Huntington's disease brain: Evidence for decreased catechol-O-methyltransferase activity

M. Hayden, E. Mcgeer, B. Kremer, 1993, Biological Psychiatry.

Acute cerebral perfusion CT abnormalities associated with posttraumatic amnesia in mild head injury.

B. Kremer, B. D. de Jong, J. van der Naalt, 2010, Journal of neurotrauma.

Cognitive impairment in SCA-19.

H. J. Schelhaas, B. Kremer, G. Hageman, 2003, Acta neurologica Belgica.

Near Infrared Spectroscopy for the Detection of Desaturations in Vulnerable Ischemic Brain Tissue: A Pilot Study at the Stroke Unit Bedside

M. Aries, B. Kremer, J. Elting, 2012, Stroke.

NMDA receptor gene variations as modifiers in Huntington disease: a replication study

J. Schiefer, R. Barker, R. Reilmann, 2011, PLoS currents.

P 115. Effects of rTMS in conversion paralysis

B. Kremer, H. V. D. Hoeven, M. Beilen, 2013, Clinical Neurophysiology.

Prevalence of intronic repeat expansions in RFC1 in Dutch patients with CANVAS and adult-onset ataxia

B. Kremer, J. D. de Vries, R. van de Berg, 2022, Journal of Neurology.

Cerebral Amyloid Angiopathy with Severe Secondary Vascular Pathology: A Histopathological Study

P. Wesseling, M. Verbeek, B. Kremer, 2005, Dementia and Geriatric Cognitive Disorders.

Falls in Spinocerebellar Ataxias: Results of the EuroSCA Fall Study

Paola Giunti, Bastiaan R. Bloem, Massimo Pandolfo, 2010, The Cerebellum.

Cerebrospinal fluid Aβ42 levels in multiple system atrophy

W. F. Abdo, B. Bloem, M. Horstink, 2004, Movement disorders : official journal of the Movement Disorder Society.

The hypothalamic lateral tuberal nucleus in Alzheimer's disease

R. Ravid, D. Swaab, B. Kremer, 1991, Annals of neurology.

Erratum: Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm

M. Hayden, B. Kremer, S. Andrew, 1994, Nature Genetics.

The mitochondrial toxin 3‐nitropropionic acid induces differential expression patterns of apoptosis‐related markers in rat striatum

M. Verbeek, B. Kremer, R. D. de Waal, 2001, Neuropathology and applied neurobiology.

Somatic mosaicism in sperm is associated with intergenerational (CAG)n changes in Huntington disease.

B. Kremer, F. Squitieri, E. Almqvist, 1995, Human molecular genetics.

Imminent brain death: point of departure for potential heart-beating organ donor recognition

A. Maas, M. Kuiper, E. Wijdicks, 2010, Intensive Care Medicine.

Chromosome instability predicts the progression of premalignant oral lesions.

J. A. van der Laak, E. Speel, B. Kremer, 2013, Oral oncology.

University of Groningen Functional Analysis Helps to Define KCNC 3 Mutational Spectrum in Dutch Ataxia Cases

R. Sinke, B. Kremer, E. Boddeke, 2018 .

Variations of blood pressure in stroke unit patients may result from alternating body positions.

M. Aries, B. Kremer, J. De Keyser, 2012, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes.

W. Robberecht, L. H. van den Berg, J. Veldink, 2009, Archives of neurology.

Co-occurrence of X-Linked Congenital Adrenal Hypoplasia and Autistic Disorder

B. Kremer, P. Naarding, M. Smits, 2009 .

Neuropathology in classical and variant ataxia‐telangiectasia

B. Kremer, M. van Deuren, M. Willemsen, 2012, Neuropathology (Kyoto. 1993).

Language impairment in cerebellar ataxia

B. Kremer, S. Knuijt, J. Gaalen, 2014, Movement disorders : official journal of the Movement Disorder Society.

Cerebral blood flow velocity changes during upright positioning in bed after acute stroke: an observational study

M. Aries, B. Kremer, J. De Keyser, 2013, BMJ Open.

Diffusion tensor imaging and tractography of the white matter in normal aging: The rate-of-change differs between segments within tracts.

Danielle van Westen, J. Lätt, D. Westen, 2018, Magnetic resonance imaging.

Neurophysiologic Studies in Early-Onset Cerebellar Ataxia

M. Zwarts, H. J. Schelhaas, B. Kremer, 2006, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.