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Variability and validity of polymorphism association studies in Parkinson's disease

Neurology, 2000-08, Vol.55 (4), p.533-538

2000

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P02-130 - Characteristic prefrontal blood volume patterns when imaging body type, high-calorie food, and mother-child attachment in childhood anorexia nervosa: A near infrared spectroscopy study

European psychiatry, 2011, Vol.26, p.726-726

2011

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Polymorphism of NACP-Rep1 in Parkinson's disease: an etiologic link with essential tremor?

Neurology, 2000-03, Vol.54 (5), p.1195-1198

2000

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A "dystrophic" variant of autosomal recessive myotonia congenita caused by novel mutations in the CLCN1 gene

Neurology, 2000-12, Vol.55 (11), p.1697-1703

2000

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Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome

Journal of medical genetics, 2000-08, Vol.37 (8), p.608-610

2000

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Extrapontine myelinolysis with parkinsonism after rapid correction of hyponatremia: high cerebrospinal fluid level of homovanillic acid and successful dopaminergic treatment

Journal of Neural Transmission, 1999-01, Vol.106 (9-10), p.949-953

1999

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Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan

Brain & development (Tokyo. 1979), 2010-06, Vol.32 (6), p.454-462

2010

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Decreased cerebellar blood flow in postinfectious acute cerebellar ataxia

Journal of neurology, neurosurgery and psychiatry, 1999-07, Vol.67 (1), p.109-112

1999

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Decreased cerebrospinal fluid levels of β-endorphin and ACTH in children with infantile spasms

Journal of Neural Transmission, 2001-01, Vol.108 (3), p.363-371

2001

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Alcohol dehydrogenase polymorphism and Parkinson's disease

Neuroscience letters, 2001-06, Vol.305 (1), p.70-72

2001

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Severe infantile measles encephalitis occurred three months after neonatal measles

Neuropediatrics, 2002-10, Vol.33 (5), p.274-277

2002

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Increased cerebrospinal fluid levels of substance P in patients with amyotrophic lateral sclerosis

Journal of Neural Transmission, 1999-10, Vol.106 (9-10), p.943-948

1999

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Characteristic prefrontal blood volume patterns when imaging body type, high-calorie food, and mother-child attachment in childhood anorexia nervosa: A near infrared spectroscopy study

European psychiatry, 2011-03, Vol.26 (S2), p.726-726

2011

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Decreased CSF levels of substance P in patients with congenital sensory neuropathy with anhidrosis

Neurology, 1997-04, Vol.48 (4), p.1133-1133

1997

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Paroxysmal Kinesigenic Choreoathetosis Locus Maps to Chromosome 16p11.2-q12.1

American journal of human genetics, 1999-12, Vol.65 (6), p.1688-1697

1999

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Elevated cerebrospinal fluid lactate/pyruvate ratio in Machado-Joseph disease

Acta neurologica Scandinavica, 1996-01, Vol.93 (1), p.72-75

1996

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Age-related changes in the cerebrospinal fluid level of β-endorphin and substance P

Journal of Neural Transmission, 1998, Vol.105 (1), p.53-58

1998

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PREFRONTAL BRAIN FUNCTION IN PATIENTS WITH EATING DISORDERS: A NEAR-INFRARED SPECTROSCOPY STUDY

Neuropediatrics, 2006, Vol.37 (S 1)

2006

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Methyl-CpG binding protein 2 gene ( MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms

Brain & development (Tokyo. 1979), 2005-04, Vol.27 (3), p.211-217

2005

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Clinical experience of gallbladder and biliary cancer, with special reference to the early stage

Naika, 1971-04, Vol.27 (4), p.678

Nagamitsu, S

1971

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Reconstructive surgery of the bile duct

Shujutsu. Operation, 1969-11, Vol.23 (11), p.1371

Nagamitsu, S

1969

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ON VARIOUS PROBLEMS ON MECHANISM OF DEVELOPMENT OF BILIARY CALCULI

Fukuoka igaku zasshi = Hukuoka acta medica, 1964-02, Vol.55, p.69

NAGAMITSU, S

1964

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THE FIRST SUMMER TREATMENT PROGRAM FOR CHILDREN WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER IN KURUME CITY, JAPAN

Neuropediatrics, 2006, Vol.37 (S 1)

2006

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Multicenter study of paroxysmal dyskinesias in Japan-Clinical and pedigree analysis

Movement disorders, 1999-07, Vol.14 (4), p.658-663

1999

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Decreased cerebrospinal fluid levels of substance P in patients with Rett syndrome

Annals of neurology, 1997-12, Vol.42 (6), p.978-981

1997

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Variability and validity of polymorphism association studies in Parkinson's disease

P02-130 - Characteristic prefrontal blood volume patterns when imaging body type, high-calorie food, and mother-child attachment in childhood anorexia nervosa: A near infrared spectroscopy study

Polymorphism of NACP-Rep1 in Parkinson's disease: an etiologic link with essential tremor?

A "dystrophic" variant of autosomal recessive myotonia congenita caused by novel mutations in the CLCN1 gene

Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome

Extrapontine myelinolysis with parkinsonism after rapid correction of hyponatremia: high cerebrospinal fluid level of homovanillic acid and successful dopaminergic treatment

Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan

Decreased cerebellar blood flow in postinfectious acute cerebellar ataxia

Decreased cerebrospinal fluid levels of β-endorphin and ACTH in children with infantile spasms

Alcohol dehydrogenase polymorphism and Parkinson's disease

Severe infantile measles encephalitis occurred three months after neonatal measles

Increased cerebrospinal fluid levels of substance P in patients with amyotrophic lateral sclerosis

Characteristic prefrontal blood volume patterns when imaging body type, high-calorie food, and mother-child attachment in childhood anorexia nervosa: A near infrared spectroscopy study

Decreased CSF levels of substance P in patients with congenital sensory neuropathy with anhidrosis

Paroxysmal Kinesigenic Choreoathetosis Locus Maps to Chromosome 16p11.2-q12.1

Elevated cerebrospinal fluid lactate/pyruvate ratio in Machado-Joseph disease

Age-related changes in the cerebrospinal fluid level of β-endorphin and substance P

PREFRONTAL BRAIN FUNCTION IN PATIENTS WITH EATING DISORDERS: A NEAR-INFRARED SPECTROSCOPY STUDY

Methyl-CpG binding protein 2 gene ( MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms

Clinical experience of gallbladder and biliary cancer, with special reference to the early stage

Reconstructive surgery of the bile duct

ON VARIOUS PROBLEMS ON MECHANISM OF DEVELOPMENT OF BILIARY CALCULI

THE FIRST SUMMER TREATMENT PROGRAM FOR CHILDREN WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER IN KURUME CITY, JAPAN

Multicenter study of paroxysmal dyskinesias in Japan-Clinical and pedigree analysis

Decreased cerebrospinal fluid levels of substance P in patients with Rett syndrome

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