H. Kawai

发表

[A clinicopathological investigation of two autopsy cases of calpainopathy (LGMD2A)].

Shuji Hashiguchi, K. Adachi, T. Inui, 2014, Brain and nerve = Shinkei kenkyu no shinpo.

Clinical, pathological, and genetic features of limb‐girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese families

J. Beckmann, T. Fujiwara, I. Richard, 1998, Muscle & nerve.

Lysosomal enzyme activities in skeletal muscle of patients with neuromuscular diseases

S. Kashiwagi, H. Kawai, M. Kunishige, 1995, Muscle & nerve.

Increased replication of HTLV‐I in HTLV‐I–associated myelopathy

S. Sonoda, M. Osame, S. Ijichi, 1989, Annals of neurology.

Radioimmunoassay for human myoglobin: methods and results in patients with skeletal muscle or myocardial disorders.

H. Kawai, K. Miyoshi, S. Saito, 1978, The Journal of laboratory and clinical medicine.

A sensitive sandwich enzyme immunoassay for human myoglobin using Fab'-horseradish peroxidase conjugate: methods and results in normal subjects and patients with various diseases.

H. Kawai, Y. Nishida, H. Nishino, 1985, Clinica chimica acta; international journal of clinical chemistry.

Cardiac dysfunction with Becker muscular dystrophy.

M. Akaike, K. Adachi, M. Saito, 1996, American heart journal.

Characterization of the human MANB gene encoding lysosomal α -d-mannosidase

N. Wakamatsu, H. Kawai, S. Saito, 1997 .

Missense and Nonsense Mutations in the Lysosomal α-Mannosidase Gene (MANB) in Severe and Mild Forms of α-Mannosidosis

Toshio Matsumoto, N. Wakamatsu, H. Kawai, 1998 .

Acute neurotoxicity ofl-glutamate induced by impairment of the glutamate uptake system

S. Okazaki, H. Kawai, Y. Nishida, 1996, Neurochemical Research.

Different secretion profiles of atrial and brain natriuretic peptides after acute volume loading in patients with ischemic heart disease.

M. Akaike, T. Nishiuchi, H. Kawai, 1997, Acta cardiologica.

Evidence of HTLV-I in thyroid tissue in an HTLV-I carrier with Hashimoto's thyroiditis

T. Mitsui, M. Akaike, K. Hizawa, 1996, Journal of Molecular Medicine.

HTLV‐I infection in patients with autoimmune thyroiditis (Hashimoto's thyroiditis)

T. Inui, S. Kashiwagi, H. Kawai, 1992, Journal of medical virology.

Hashimoto's thyroiditis in HTLV-I carriers.

K. Hizawa, Y. Arii, H. Kawai, 1992, Internal medicine.

Mutations producing premature termination of translation and an amino acid substitution in the sterol 27-hydroxylase gene cause cerebrotendinous xanthomatosis associated with parkinsonism

S. Tsuji, N. Wakamatsu, H. Kawai, 1999, Journal of neurology, neurosurgery, and psychiatry.

Localization and amount of myoglobin and myoglobin mRNA in ragged‐red fiber of patients with mitochondrial encephalomyopathy

T. Mitsui, M. Akaike, M. Shono, 1996, Muscle & nerve.

High frequencies of human T-lymphotropic virus type I (HTLV-I) infection and presence of HTLV-II proviral DNA in blood donors with anti-thyroid antibodies

M. Akaike, H. Kawai, S. Saito, 1996, Journal of Molecular Medicine.

Plasma levels of brain natriuretic peptide as an index for evaluation of cardiac function in female gene carriers of Duchenne muscular dystrophy.

M. Akaike, T. Inui, S. Kashiwagi, 1997, Internal medicine.

Effects of calcitonin gene‐related peptide and interleukin 6 on myoblast differentiation

S. Okazaki, Y. Arii, H. Kawai, 1996, Cell proliferation.

Graves' disease in HTLV-I carriers

M. Akaike, M. Abe, H. Kawai, 1995, Journal of Molecular Medicine.

Detection and management of cardiomyopathy in female dystrophinopathy carriers

M. Akaike, T. Iwase, S. Takao, 2017, Journal of the Neurological Sciences.

HTLV‐I‐associated myelopathy with adult T‐cell leukemia

H. Kawai, Y. Nishida, S. Saito, 1989, Neurology.

Localization of myoglobin in human muscle cells by immunoelectron microscopy

H. Kawai, Y. Nishida, H. Nishino, 1987, Muscle & nerve.

Skeletal muscle pathology of mannosidosis in two siblings with spastic paraplegia

T. Inui, H. Kawai, Y. Nishida, 2004, Acta Neuropathologica.

[Estimation of cardiac function by plasma concentration of brain natriuretic peptide in patients with Duchenne muscular dystrophy].

M. Akaike, K. Adachi, S. Kashiwagi, 1996, Rinsho shinkeigaku = Clinical neurology.

[Clinical feature and mechanism of cardiac failure in patients with Becker muscular dystrophy].

M. Akaike, H. Kawai, K. Adachi, 1994, Rinsho shinkeigaku = Clinical neurology.

[Secretion and clinical significance of atrial natriuretic peptide in patients with muscular dystrophy].

T. Nishiuchi, K. Adachi, H. Kawai, 1989, Rinsho shinkeigaku = Clinical neurology.

Different manners of sarcoglycan expression in genetically proven α-sarcoglycan deficiency and γ-sarcoglycan deficiency

K. Arimura, M. Nakagawa, M. Osame, 1998, Acta Neuropathologica.

Different manners of sarcoglycan expression in genetically proven alpha-sarcoglycan deficiency and gamma-sarcoglycan deficiency.

K. Arimura, M. Nakagawa, M. Osame, 1998, Acta Neuropathologica.

Isozyme pattern of leukocyte α-d-mannosidase in patients with mannosidosis

H. Kawai, Y. Nishida, H. Nishino, 1988, Japanese Journal of Human Genetics.

Presence of human T‐lymphotropic virus type II‐related genes in DNA of peripheral leukocytes from patients with autoimmune thyroid diseases

H. Kawai, Masashi Akaike, K. Yokoi, 1995, Journal of medical virology.

[Cardiac dysfunction in female gene carriers of Duchenne muscular dystrophy].

K. Adachi, H. Kawai, T. Naruo, 1995, Rinsho shinkeigaku = Clinical neurology.

Decrease in urinary excretion of 3-methylhistidine by patients with Duchenne muscular dystrophy during glucocorticoid treatment

K. Adachi, T. Inui, H. Kawai, 2004, Journal of Neurology.

HTLV-I-associated myelopathy (HAM) in Tokushima Prefecture--geographical and clinical studies in an area between endemic and non-endemic areas of HTLV-I infection.

T. Inui, S. Kashiwagi, H. Kawai, 1991, Japanese journal of medicine.

Preferential Subsarcolemmal Localization of Dystrophin and β‐dystroglycan mRNA in Human Skeletal Muscles

T. Mitsui, H. Kawai, M. Kunishige, 1997, Journal of neuropathology and experimental neurology.

Oxidative damage to skeletal muscle DNA from patients with mitochondrial encephalomyopathies

T. Mitsui, M. Nagasawa, M. Akaike, 1996, Journal of the Neurological Sciences.

X-linked dominant control of F-cells in normal adult life: characterization of the Swiss type as hereditary persistence of fetal hemoglobin regulated dominantly by gene(s) on X chromosome.

H. Kawai, K. Miyoshi, T. Yamano, 1988, Blood.

Myoglobin Subfractions: Abnormality in Duchenne Type of Progressive Muscular Dystrophy

H. Kawai, K. Miyoshi, K. Saijo, 1968, Science.

Characteristic properties of fetal human albumin (Alb F) in isomerization equilibrium.

H. Kawai, K. Miyoshi, K. Saijo, 1966, The Tokushima journal of experimental medicine.

Characterization of the human MANB gene encoding lysosomal alpha-D-mannosidase.

N. Wakamatsu, H. Kawai, S. Saito, 1997, Gene.

Eosinophilic Polymyositis Induced by Tranilast

S. Arase, Y. Urano, H. Kawai, 1990, The Journal of dermatology.

Experimental glycerol myopathy: a histological study

Y. Tamaki, H. Kawai, H. Nishino, 2004, Acta Neuropathologica.

[Serum myoglobin levels following administration of succinylcholine during nitrous oxide-oxygen-halothane anesthesia (author's transl)].

H. Kawai, K. Miyoshi, A. Kondo, 1980, Masui. The Japanese journal of anesthesiology.

In situ hybridization of myoglobin mRNA: results on the skeletal muscles of normal subjects and patients with neuromuscular diseases

T. Mitsui, H. Kawai, H. Nishino, 2004, Acta Neuropathologica.

Expression of myoglobin gene in skeletal muscle of patients with neuromuscular diseases

T. Mitsui, H. Kawai, Y. Nishida, 1994, Muscle & nerve.

Mitochondrial encephalomyopathy with autosomal dominant inheritance: A clinical and genetic entity of mitochondrial diseases

M. Akaike, H. Kawai, M. Kunishige, 1995, Muscle & nerve.

Autosomal recessive distal muscular dystrophy as a new type of progressive muscular dystrophy. Seventeen cases in eight families including an autopsied case.

H. Kawai, H Nishino, H. Nishino, 1986, Brain : a journal of neurology.

[Autosomal recessive distal muscular dystrophy--a new type of distal muscular dystrophy observed characteristically in Japan].

H. Kawai, K. Miyoshi, M. Iwasa, 1977, Nihon rinsho. Japanese journal of clinical medicine.

Cardiac dysfunction in patients with chronic progressive external ophthalmoplegia

H. Kawai, Masashi Akaike, M. Kunishige, 1994, Clinical cardiology.

Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency.

T. Fujiwara, K. Matsumura, T. Mitsui, 1995, The Journal of clinical investigation.

Laminin abnormality in severe childhood autosomal recessive muscular dystrophy.

S. Roberds, T. Mitsui, K. Azibi, 1995, Laboratory investigation; a journal of technical methods and pathology.

Quantitative analysis of immunofluorescent signals for dystrophin, beta-dystroglycan and myosin skeletal muscle by epifluorescence microscopy.

T. Mitsui, M. Shono, H. Kawai, 1999, Biotechnic & histochemistry : official publication of the Biological Stain Commission.

Clinical features, particularly those of the central nervous system, of patients with Becker's muscular dystrophy, including autopsied cases

M. Saito, H. Kawai, K. Adachi, 2010 .

G.P.12.04 Clinical features, particularly those of the central nervous system of patients with Becker muscular dystrophy, including autopsied cases

T. Sano, S. Kashiwagi, M. Saito, 2008, Neuromuscular Disorders.

Induction of dystrophin-associated proteins together with nicotinic acetylcholine receptors by denervation in the absence of dystrophin in skeletal muscles of mdx mice.

T. Mitsui, H. Kawai, M. Kunishige, 1996, Biochemical and biophysical research communications.

New missense mutation in the alpha-sarcoglycan gene in a Japanese patient with severe childhood autosomal recessive muscular dystrophy with incomplete alpha-sarcoglycan deficiency

K. Arimura, M. Nakagawa, M. Osame, 1997, Journal of the Neurological Sciences.

HTLV-I-associated myelopathy (HAM/TSP) with Hashimoto's thyroiditis.

Y. Tamaki, T. Inui, S. Kashiwagi, 1991, The Tokushima journal of experimental medicine.

[HTLV-I associated myelopathy with Hashimoto's thyroiditis--a report of two cases].

T. Inui, S. Kashiwagi, H. Kawai, 1991, Rinsho shinkeigaku = Clinical neurology.

Statistically significant differences in the number of CD24 positive muscle fibers and satellite cells between sarcoglycanopathy and age-matched Becker muscular dystrophy patients.

K. Arimura, M. Nakagawa, M. Osame, 1999, Internal medicine.

Neuroimaging study of myotonic dystrophy. I. Magnetic resonance imaging of the brain

T. Hashimoto, M. Tayama, K. Murakawa, 1995, Brain and Development.

Abnormal expression of a serine protease in human dystrophic muscle.

N. Katunuma, H. Kawai, Y. Sanada, 1978, Journal of biochemistry.

Light and electron microscopic studies on localization of myoglobin in skeletal muscle cells in neuromuscular diseases

H. Kawai, Y. Nishida, H. Nishino, 1991, Muscle & nerve.

Interferon Alpha-2a Therapy for Disseminated Intravascular Coagulation in a Patient with Blue Rubber Bleb Nevus Syndrome

H. Azuma, Y. Arii, H. Kawai, 1997, Angiology.

Autonomic hyperreflexia in pure progressive autonomic failure

T. Mitsui, H. Kawai, H. Miyamoto, 1993, Neurology.

[HTLV-I associated myelopathy (HAM) with adult T-cell leukemia (ATL)].

H. Kawai, Y. Nishida, S. Saito, 1989, Rinsho shinkeigaku = Clinical neurology.

Ultrastructural localization of myoglobin mRNA in human skeletal muscle

T. Mitsui, H. Kawai, T. Naruo, 1994, Histochemistry.

Overexpressions of myoglobin and antioxidant enzymes in ragged‐red fibers of skeletal muscle from patients with mitochondrial encephalomyopathy

T. Mitsui, M. Akaike, Toshio Matsumoto, 2003, Muscle & nerve.

Proteolysis of β-dystroglycan in muscular diseases

I. Nishino, K. Matsumura, I. Higuchi, 2005, Neuromuscular Disorders.

Neuroimaging study of myotonic dystrophy. II. MRI measurements of the brain

Hiromu Nishitani, Hisaomi Kawai, Masahito Miyazaki, 1995, Brain and Development.

[A case of Kearns-Sayre syndrome whose asymptomatic mother had abnormal mitochondria in skeletal muscle].

M. Akaike, S. Kashiwagi, H. Kawai, 1995, Rinsho shinkeigaku = Clinical neurology.

Detection and management of cardiomyopathy in female dystrophinopathy carriers

M. Akaike, T. Iwase, S. Takao, 2017, Journal of the Neurological Sciences.