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Crystalline nephropathy caused by tosufloxacin

Pediatrics international, 2016-11, Vol.58 (11), p.1219-1221

2016

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Ask-Upmark kidney in a girl with neurofibromatosis type 1

CEN case reports, 2020-08, Vol.9 (3), p.285-288

2020

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Secondary pseudohypoaldosteronism causing cardiopulmonary arrest and cholelithiasis

Pediatrics international, 2014-04, Vol.56 (2), p.270-272

2014

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C/EBPα is Required for Differentiation of White, but not Brown, Adipose Tissue

Proceedings of the National Academy of Sciences - PNAS, 2001-10, Vol.98 (22), p.12532-12537

2001

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Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state

Brain & development (Tokyo. 1979), 2015-10, Vol.37 (9), p.887-890

2015

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Lateral medullary syndrome in a boy with hereditary dysfibrinogenemia

Brain & development (Tokyo. 1979), 2012-11, Vol.34 (10), p.857-860

2012

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Neonatal renal venous thrombosis followed by secondary pseudohypoaldosteronism

Pediatrics international, 2012-12, Vol.54 (6), p.936-938

2012

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Predominant Corticospinal Tract Involvement in a Late Infant with Krabbe Disease

Japanese Clinical Medicine, 2016-01, Vol.2016 (7), p.23-26

2016

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A novel PLP mutation in a Japanese patient with mild Pelizaeus-Merzbacher disease

Brain & development (Tokyo. 1979), 2009-03, Vol.31 (3), p.248-251

2009

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Delayed gyration with pontocerebellar hypoplasia type 1

Brain & development (Tokyo. 1979), 2010-03, Vol.32 (3), p.258-262

2010

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Refractory epilepsy accompanying acute encephalitis with multifocal cortical lesions: Possible autoimmune etiology

Brain & development (Tokyo. 1979), 2007-10, Vol.29 (9), p.590-594

2007

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The Persistent Generalized Muscle Contraction in Siblings with Molybdenum Cofactor Deficiency Type A

Neuropediatrics, 2019-04, Vol.50 (2), p.126-129

2019

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Congenital dysfibrinogenemia in a Japanese family with fibrinogen Naples (BβAla68Thr) manifesting as superior sagittal sinus thrombosis

Blood coagulation & fibrinolysis, 2017-10, Vol.28 (7), p.580-584

2017

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Cervical myelopathy associated with os odontoideum after botulinum toxin treatment in a patient with cerebral palsy

No to hattatsu, 2014-07, Vol.46 (4), p.307

2014

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Congenital muscular dystrophy caused by integrin α7 deficiency

Developmental medicine and child neurology, 2009-03, Vol.51 (3), p.245-245

2009

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Predominant Corticospinal Tract involvement in a late infant with Krabbe disease

Japanese clinical medicine, 2016-09, p.1

2016

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Two concurrent chromosomal aberrations involving interstitial deletion in 1q24.2q25.2 and inverted duplication and deletion in 10q26 in a patient with stroke associated with antithrombin deficiency and a patent foramen ovale

American journal of medical genetics. Part A, 2011-01, Vol.155 (1), p.215-220

2011

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Congenital muscular dystrophy caused by integrin [alpha]7 deficiency

Developmental medicine and child neurology, 2009-03, Vol.51 (3), p.245

2009

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Diffuse central nervous system lupus involving white matter, basal ganglia, thalami and brainstem

Brain & development (Tokyo. 1979), 1999-07, Vol.21 (5), p.337-340

1999

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Glycosylation and Placental Transport of Immunoglobulin G

Journal of Clinical Biochemistry and Nutrition, 1996, Vol.21(1), pp.57-63

1996

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Congenital muscular dystrophy caused by integrin alpha7 deficiency

Developmental medicine and child neurology, 2009-03, Vol.51 (3), p.245

2009

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Serial MRI findings of benign poliomyelitis

Brain & development (Tokyo. 1979), 1996-03, Vol.18 (2), p.147-149

1996

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Crystalline nephropathy caused by tosufloxacin

Pediatrics international : official journal of the Japan Pediatric Society, 2016, Vol.58 (11), p.1219-1221

2016

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Crystalline nephropathy caused by tosufloxacin

Pediatrics International, 2016, Vol.58 (11), p.1219-1221

2016

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C/EBPalpha is required for differentiation of white, but not brown, adipose tissue

Proceedings of the National Academy of Sciences - PNAS, 2001-10, Vol.98 (22), p.12532-12537

2001

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Crystalline nephropathy caused by tosufloxacin

Ask-Upmark kidney in a girl with neurofibromatosis type 1

Secondary pseudohypoaldosteronism causing cardiopulmonary arrest and cholelithiasis

C/EBPα is Required for Differentiation of White, but not Brown, Adipose Tissue

Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state

Lateral medullary syndrome in a boy with hereditary dysfibrinogenemia

Neonatal renal venous thrombosis followed by secondary pseudohypoaldosteronism

Predominant Corticospinal Tract Involvement in a Late Infant with Krabbe Disease

A novel PLP mutation in a Japanese patient with mild Pelizaeus-Merzbacher disease

Delayed gyration with pontocerebellar hypoplasia type 1

Refractory epilepsy accompanying acute encephalitis with multifocal cortical lesions: Possible autoimmune etiology

The Persistent Generalized Muscle Contraction in Siblings with Molybdenum Cofactor Deficiency Type A

Congenital dysfibrinogenemia in a Japanese family with fibrinogen Naples (BβAla68Thr) manifesting as superior sagittal sinus thrombosis

Cervical myelopathy associated with os odontoideum after botulinum toxin treatment in a patient with cerebral palsy

Congenital muscular dystrophy caused by integrin α7 deficiency

Predominant Corticospinal Tract involvement in a late infant with Krabbe disease

Two concurrent chromosomal aberrations involving interstitial deletion in 1q24.2q25.2 and inverted duplication and deletion in 10q26 in a patient with stroke associated with antithrombin deficiency and a patent foramen ovale

Congenital muscular dystrophy caused by integrin [alpha]7 deficiency

Diffuse central nervous system lupus involving white matter, basal ganglia, thalami and brainstem

Glycosylation and Placental Transport of Immunoglobulin G

Congenital muscular dystrophy caused by integrin alpha7 deficiency

Serial MRI findings of benign poliomyelitis

Crystalline nephropathy caused by tosufloxacin

Crystalline nephropathy caused by tosufloxacin

C/EBPalpha is required for differentiation of white, but not brown, adipose tissue

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