Y. Yamamura

发表

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

S. Minoshima, N. Shimizu, N. Hattori, 1998, Nature.

Low intensity areas observed on T2-weighted magnetic resonance imaging of the cerebral cortex in various neurological diseases

Katsuhide Ito, S. Yamaguchi, Shigenobu Nakamura, 1995, Journal of the Neurological Sciences.

Autosomal recessive juvenile parkinsonism maps to 6q25.2-q27 in four ethnic groups: detailed genetic mapping of the linked region.

D. Weeks, L. Almasy, J. Hubble, 1998, American journal of human genetics.

Clinical, pathologic and genetic studies on autosomal recessive early-onset parkinsonism with diurnal fluctuation.

Y. Mizuno, S. Kuzuhara, H. Matsumine, 1998, Parkinsonism & related disorders.

Ultrastructural localization of glucose transporter 1 (GLUT1) in guinea pig stria vascularis and vestibular dark cell areas: an immunogold study.

T. Ishii, Y. Yamamura, T. Yoshihara, 1999, Acta oto-laryngologica.

Slowly progressive L-DOPA nonresponsive pure akinesia due to nigropallidal degeneration: a clinicopathological case study

S. Nakamura, E. Tahara, S. Katayama, 1998, Journal of the Neurological Sciences.

Iron accumulation in the substantia nigra of autosomal recessive juvenile parkinsonism (ARJP).

N. Hattori, H. Mochizuki, Y. Mizuno, 2001, Parkinsonism & related disorders.

Autoradiographic Distributions of Neurotransmitter Receptors in the Brain of Patients with Parkinson’s Disease and MPTP-induced Monkey Parkinsonism

Y. Yamamura, H. Matsubayashi, S. Kito, 1986 .

The long journey to the discovery of PARK2

Y. Yamamura, 2010, Neuropathology : official journal of the Japanese Society of Neuropathology.

Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene.

A. Brookes, S. Minoshima, N. Shimizu, 1998, Biochemical and biophysical research communications.

[Autosomal recessive early-onset parkinsonism with diurnal fluctuation (AR-EPDF)--clinical characteristics].

S. Nakamura, H. Kawakami, T. Kohriyama, 1996, Rinsho shinkeigaku = Clinical neurology.

[Early-onset parkinsonism with diurnal fluctuation--clinical and pathological studies].

K. Arihiro, S. Nakamura, T. Kohriyama, 1993, Rinsho shinkeigaku = Clinical neurology.

Mapping of somatostatin receptor localization in rat brain: Forebrain and diencephalon

S. Katayama, Y. Yamamura, S. Kito, 1990, Brain Research Bulletin.

PARKIN as a pathogenic gene for autosomal recessive juvenile parkinsonism.

Y Mizuno, S Minoshima, Y Yamamura, 2000, Journal of neural transmission. Supplementum.

Effects of nicotine chewing gum on UPDRS score and P300 in early-onset parkinsonism.

H. Kawakami, T. Kohriyama, Shigenobu Nakamura, 2002, Hiroshima journal of medical sciences.

Numerous conglomerate inclusions in slowly progressive familial amyotrophic lateral sclerosis with posterior column involvement

S. Murayama, S. Katayama, Shigenobu Nakamura, 1999, Journal of the Neurological Sciences.

Pure autonomic failure with motor neuron disease: report of a clinical study and postmortem examination of a patient.

S. Nakamura, S. Katayama, Y. Yamamura, 1996, Journal of neurology, neurosurgery, and psychiatry.

A microdeletion of D6S305 in a family of autosomal recessive juvenile parkinsonism (PARK2).

Y Mizuno, Y Yamamura, N. Hattori, 1998, Genomics.

[The effect of age and disease on the MR imaging T2 low signal intensity area in the cerebral cortex].

S. Nakamura, S. Yamaguchi, S. Katayama, 1994, Nihon Ronen Igakkai zasshi. Japanese journal of geriatrics.

CLINICAL MANIFESTATIONS OF AUTOSOMAL RECESSIVE EARLY-ONSET PARKINSONISM WITH DIURNAL FLUCTUATION

H. Kawakami, T. Kohriyama, S. Katayama, 1996 .

Increased frequency of antigen-specific CD8(+) cytotoxic T lymphocytes infiltrating an Epstein-Barr virus-associated gastric carcinoma.

S. Nakamura, M. Fujita, T. Kiyono, 1999, The Journal of clinical investigation.

[Fine structure of intrafusal and extrafusal nerve segments of the rat muscle spindle after sciatic nerve transsection].

R. Schober, Y. Yamamura, 1983, Acta neuropathologica.

Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in the Parkin gene in affected individuals

N. Shimizu, N. Hattori, S. Asakawa, 1998, Annals of neurology.

Novel PINK1 mutations in early‐onset parkinsonism

Nobutaka Hattori, Yoshikuni Mizuno, Hiroyuki Tomiyama, 2004, Annals of neurology.

Malignant lymphoma presenting with neoplastic angioendotheliosis of the central nervous system.

Y. Yamamura, S. Kito, T. Hamada, 1983, Clinical neuropathology.

n‐Hexane Polyneuropathy †

Y. Yamamura, Y. Yamamura, 1969, Folia psychiatrica et neurologica japonica.

Immunohistochemical and subcellular localization of parkin protein: Absence of protein in autosomal recessive juvenile parkinsonism patients

S. Minoshima, N. Shimizu, N. Hattori, 1999, Annals of neurology.

Alteration of muscarinic receptor subtypes in CA1 field of hippocampus in senile dementia of Alzheimer type: an autoradiographic study.

I. Kanazawa, S. Katayama, Y. Yamamura, 1990, Hiroshima journal of medical sciences.

[A case of idiopathic superficial siderosis of the central nervous system].

S. Nakamura, S. Yamaguchi, Z. Matsuyama, 1994, No to shinkei = Brain and nerve.

Treatment by pacemaker in familial amyloid polyneuropathy.

M. Yamada, Y. Yamamura, K. Akiyama, 1989, Chest.

“Pure” Suprasellar Schwannoma Presented with Communicating Hydrocephalus: A Case Report

H. Namba, Y. Yamamura, S. Ito, 2017, NMC case report journal.

Effects of anticholinergic antiparkinsonian drugs on binding of muscarinic receptor subtypes in rat brain.

F. Ishizaki, S. Katayama, Y. Yamamura, 1990, Research communications in chemical pathology and pharmacology.

Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27.

A A Schäffer, Y Mizuno, Y Yamamura, 1997, American journal of human genetics.

a Chromosome 6q-Linked Parkinsonism

S. Tsuji, Y. Mizuno, H. Matsumine, 1998 .

Myeloneuropathy with abdominal disorders in Japan

T. Takayanagi, Y. Yamamura, Y. Matsuoka, 1971, Neurology.

Point Mutations (Thr240Arg and Ala311Stop) in theParkinGene

A. Brookes, S. Minoshima, N. Shimizu, 1998 .

Autosomal recessive early-onset parkinsonism with diurnal fluctuation: clinicopathologic characteristics and molecular genetic identification

N. Hattori, Y. Mizuno, S. Kuzuhara, 2000, Brain and Development.

Paralysis agitans of early onset with marked diurnal fluctuation of symptoms

Y. Yamamura, I. Sobue, T. Yanagi, 1973, Neurology.

Studies on familial amyloid polyneuropathy in Ogawa Village, Japan.

Y. Yamamura, S. Kito, E. Itoga, 1980, European neurology.

Natural History of Ogawa Village Type Familial Amyloid Polyneuropathy in Japan

S. Katayama, Y. Yamamura, S. Kito, 1988 .

Immunohistochemical Studies on Autopsied Organs of Familial Amyloid Polyneuropathy in Relation with Amyloid Protein

Y. Yamamura, S. Kito, R. Miyoshi, 1986 .

Cardiac Disorders and Autonomic Nervous System Involvement in Familial Amyloidosis

Y. Yamamura, H. Matsubayashi, S. Kito, 1986 .

PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations

N. Hattori, H. Yoshino, R. Rosales, 2004, Neurology.

Early onset parkinsonism with diurnal fluctuation maps to a locus for juvenile parkinsonism

S. Nakamura, Shigenobu Nakamura, Y. Mizuno, 1998, Neurology.

The relationship between αB‐crystallin and neurofibrillary tangles in Alzheimer's disease

S. Nakamura, S. Katayama, Y. Yamamura, 2001 .

Gallyas- and tau-positive glial structures in motor neuron disease with dementia.

S. Nakamura, S. Katayama, Y. Yamamura, 1999, Clinical neuropathology.

Hirano bodies in the axon of peripheral nerves in a case with progressive external ophthalmoplegia with multisystemic involvements

Y. Yamamura, F. Ikuta, T. Atsumi, 2004, Acta Neuropathologica.

Gallyas-positive argyrophilic and ubiquitinated filamentous inclusions in rapidly progressive motor neuron disease: immunohistochemical and electron microscopic studies

S. Nakamura, T. Kohriyama, S. Katayama, 2000, Acta Neuropathologica.

A decrease in cerebral cortex intensity on T2-weighted with ageing images of normal subjects

S. Nakamura, Y. Murata, S. Yamaguchi, 1998, Neuroradiology.

The relationship between alphaB-crystallin and neurofibrillary tangles in Alzheimer's disease.

S. Nakamura, S. Katayama, Y. Yamamura, 2001, Neuropathology and applied neurobiology.

S. Nakamura, S. Yamaguchi, T. Kohriyama, 1996 .

Parkinsonism of early-onset with diurnal fluctuation

Y. Yamamura, 1993 .

Decrease of neurons in the medullary arcuate nucleus of multiple system atrophy: quantitative comparison with Parkinson's disease and amyotrophic lateral sclerosis

S. Katayama, Shigenobu Nakamura, Y. Yamamura, 1997, Journal of the Neurological Sciences.