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Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33

Nature genetics, 1993-11, Vol.5 (3), p.283-286

1993

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Demonstration of cathepsins B, H and L in xenografts of normal and Duchenne-muscular-dystrophy muscles transplanted into nude mice

Biochemical journal, 1992-12, Vol.288 (2), p.643-648

1992

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Freeze-fracture analysis of muscle plasma membrane in Becker's muscular dystrophy

Neuropathology and applied neurobiology, 1994-10, Vol.20 (5), p.487-494

1994

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A STUDY ON SENSE OF EGO IDENTITY IN ADULT WOMEN: From the viewpoint of relationship with interdependent·independent construal of the self

The Japanese Journal of Educational Psychology, 1998/06/30, Vol.46(2), pp.229-239

MISUGI, Naho

1998

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Atopic dermatitis and related factors observed at infant physical examination at health centers

Nihon kōshū eisei zasshi, 1997-05, Vol.44 (5), p.384-390

1997

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Congenital polyneuropathy in Walker-Warburg syndrome

Neuropediatrics, 1992-02, Vol.23 (1), p.14-17

1992

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A case of motor and sensory neuropathy associated with metatropic dysplasia

No to hattatsu, 1994-05, Vol.26 (3), p.258

1994

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High-resolution banding study of an X/4 translocation in a female with Duchenne muscular dystrophy

Human genetics, 1985-01, Vol.71 (4), p.370-371

1985

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The pancreatic islet of infants with severe hypoglycemia

Archives of pathology (1960), 1970-03, Vol.89 (3), p.208

1970

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Detection of dystrophin with anti-peptide antibodies

Rinsho byori. The Japanese journal of clinical pathology, 1992-09, Vol.40 (9), p.953

1992

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Pancreatic islets of infants with severe hypoglycemia as revealed by silver stains

Yokohama medical bulletin, 1970-02, Vol.21 (1), p.1

1970

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Expression of Selectin Families and Their Ligand Sialyl Lewis X in the Muscles of Inflammatory Myopathies: An Immunohistochemical Study

Internal Medicine, 1999, Vol.38(8), pp.632-635

1999

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Ultrastructure of a so-called granular cell myoblastoma

Yokohama medical bulletin, 1967-12, Vol.18 (6), p.225

1967

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Light and electron microscopic studies of congenital muscular dystrophy

Brain & development (Tokyo. 1979), 1980, Vol.2 (2), p.191-199

Misugi, Nobuko

1980

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Fukuyama-type congenital muscular dystrophy and the Walker-Warburg syndrome

Brain & development (Tokyo. 1979), 1993-05, Vol.15 (3), p.182-191

1993

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Fine structural study of neuroblastoma, ganglioneuroblastoma, and pheochromocytoma

Archives of pathology (1960), 1968-08, Vol.86 (2), p.160

1968

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Dystrophin immunostaining and freeze-fracture studies of muscles of patients with early stage amyotrophic lateral sclerosis and Duchenne muscular dystrophy

Journal of the neurological sciences, 1989-06, Vol.91 (1), p.191-205

1989

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Altered distribution of β-Dystroglycan in sarcolemma of human dystrophic muscles: An immunohistochemical study

Muscle & nerve, 1995-08, Vol.18 (8), p.910-913

1995

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Immunoreactivity of antibodies raised against synthetic peptide fragments predicted from mid portions of dystrophin cDNA

Journal of the neurological sciences, 1990-07, Vol.97 (2), p.241-250

1990

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A case of non-Fukuyama type congenital muscular dystrophy with progression in early adulthood, ocular involvement, and sensorineural deafness

Rinshō shinkeigaku, 1993-04, Vol.33 (4), p.405

1993

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Diaphragm muscle pathology in Fukyama type congenital muscular dystrophy

Brain & development (Tokyo. 1979), 1990, Vol.12 (6), p.779-783

1990

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Diaphragm muscle pathology in fukuyama type congenital muscular dystrophy

Brain & development (Tokyo. 1979), 1990, Vol.12 (6), p.779-783

1990

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Classification of primary malignant tumors of liver in infancy and childhood

Cancer, 1967-10, Vol.20 (10), p.1760-1771

1967

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Clinical features in a girl with Duchenne muscular dystrophy with an X-autosome translocation; (X;4)(p21;q26)

Brain & development (Tokyo. 1979), 1986, Vol.8 (6), p.619-623

1986

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Peripheral nerve pathology in infantile neuroaxonal dystrophy

No to hattatsu, 1986-01, Vol.18 (1), p.8

1986

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Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33

Demonstration of cathepsins B, H and L in xenografts of normal and Duchenne-muscular-dystrophy muscles transplanted into nude mice

Freeze-fracture analysis of muscle plasma membrane in Becker's muscular dystrophy

A STUDY ON SENSE OF EGO IDENTITY IN ADULT WOMEN: From the viewpoint of relationship with interdependent·independent construal of the self

Atopic dermatitis and related factors observed at infant physical examination at health centers

Congenital polyneuropathy in Walker-Warburg syndrome

A case of motor and sensory neuropathy associated with metatropic dysplasia

High-resolution banding study of an X/4 translocation in a female with Duchenne muscular dystrophy

The pancreatic islet of infants with severe hypoglycemia

Detection of dystrophin with anti-peptide antibodies

Pancreatic islets of infants with severe hypoglycemia as revealed by silver stains

Expression of Selectin Families and Their Ligand Sialyl Lewis X in the Muscles of Inflammatory Myopathies: An Immunohistochemical Study

Ultrastructure of a so-called granular cell myoblastoma

Light and electron microscopic studies of congenital muscular dystrophy

Fukuyama-type congenital muscular dystrophy and the Walker-Warburg syndrome

Fine structural study of neuroblastoma, ganglioneuroblastoma, and pheochromocytoma

Dystrophin immunostaining and freeze-fracture studies of muscles of patients with early stage amyotrophic lateral sclerosis and Duchenne muscular dystrophy

Altered distribution of β-Dystroglycan in sarcolemma of human dystrophic muscles: An immunohistochemical study

Immunoreactivity of antibodies raised against synthetic peptide fragments predicted from mid portions of dystrophin cDNA

A case of non-Fukuyama type congenital muscular dystrophy with progression in early adulthood, ocular involvement, and sensorineural deafness

Diaphragm muscle pathology in Fukyama type congenital muscular dystrophy

Diaphragm muscle pathology in fukuyama type congenital muscular dystrophy

Classification of primary malignant tumors of liver in infancy and childhood

Clinical features in a girl with Duchenne muscular dystrophy with an X-autosome translocation; (X;4)(p21;q26)

Peripheral nerve pathology in infantile neuroaxonal dystrophy

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