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Clinically-oriented monitoring of acute effects of methylphenidate on cerebral hemodynamics in ADHD children using fNIRS

Clinical neurophysiology, 2012-06, Vol.123 (6), p.1147-1157

2012

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Polyglutamine aggregates stimulate ER stress signals and caspase-12 activation

Human molecular genetics, 2002-06, Vol.11 (13), p.1505-1515

2002

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Blood chimerism in monochorionic twins conceived by induced ovulation: Case report

Human reproduction (Oxford), 2006-03, Vol.21 (3), p.735-737

2006

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A complex of synaptic adhesion molecule CADM1, a molecule related to autism spectrum disorder, with MUPP1 in the cerebellum

Journal of neurochemistry, 2012-12, Vol.123 (5), p.886-894

2012

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Effects of high-dose intravenous corticosteroid therapy in Landau-Kleffner syndrome

Pediatric neurology, 2000-02, Vol.22 (2), p.145-147

2000

Volltextzugriff (PDF)

Acute Infantile Encephalopathy Predominantly Affecting the Frontal Lobes

Pediatric neurology, 2006-02, Vol.34 (2), p.93-100

2006

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Clinical features of neonatal toxic shock syndrome-like exanthematous disease emerging in Japan

The Journal of infection, 2009-09, Vol.59 (3), p.194-200

2009

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Two New XPD Patients Compound Heterozygous for the Same Mutation Demonstrate Diverse Clinical Features

Journal of investigative dermatology, 2005-07, Vol.125 (1), p.86-92

2005

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Splice site mutation in the hepatocyte nuclear factor-1β gene, IVS2nt + 1G > A, associated with maturity-onset diabetes of the young, renal dysplasia and bicornuate uterus

Diabetologia, 2001-03, Vol.44 (3), p.387-388

2001

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Effects of dichloroacetate in three patients with MELAS

Neurology, 1998-02, Vol.50 (2), p.531

1998

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Efficacy of Iodine-123-15-(p-iodophenyl)-3-R, S-Methylpentadecanoic Acid Single Photon Emission Computed Tomography Imaging in Detecting Myocardial Ischemia in Children With Kawasaki Disease

Circulation Journal, 2003, Vol.67(8), pp.663-666

2003

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High serum levels of M‐CSF and G‐CSF in Kawasaki disease

British journal of haematology, 1999-06, Vol.105 (3), p.613-615

1999

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Various types of LRP5 mutations in four patients with osteoporosis-pseudoglioma syndrome: Identification of a 7.2-kb microdeletion using oligonucleotide tiling microarray

American journal of medical genetics. Part A, 2010-01, Vol.152A (1), p.133-140

2010

Volltextzugriff (PDF)

Acute disseminated encephalomyelitis after live rubella vaccination

Brain & development (Tokyo. 1979), 2000-06, Vol.22 (4), p.259-261

2000

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Panipenem-betamipron and decreases in Serum valproic acid concentration

Therapeutic drug monitoring, 1998-08, Vol.20 (4), p.396-400

1998

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Cost effectiveness of prophylactic treatment with activated prothrombin complex concentrate in a patient with inhibitor-positive hemophilia A

Blood coagulation & fibrinolysis, 2012-04, Vol.23 (3), p.235-237

2012

Volltextzugriff (PDF)

Respiration-deficient cells are caused by a single point mutation in the mitochondrial tRNA-Leu (UUR) gene in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)

American journal of human genetics, 1991-09, Vol.49 (3), p.590-599

1991

Volltextzugriff (PDF)

Prenatal MRI in a fetus with a giant neck hemangioma: a case report

Prenatal diagnosis, 2000-12, Vol.20 (12), p.1004-1007

2000

Volltextzugriff (PDF)

Mutational analysis of the BMP-1 gene in patients with gastroschisis

Journal of pediatric surgery, 2001-06, Vol.36 (6), p.885-887

2001

Volltextzugriff (PDF)

Early-Onset Ataxia With Oculomotor Apraxia With a Novel APTX Mutation

Pediatric neurology, 2005-07, Vol.33 (1), p.53-56

2005

Volltextzugriff (PDF)

Drop episodes in Coffin-Lowry syndrome: exaggerated startle responses treated with clonazepam

Pediatric neurology, 1998-08, Vol.19 (2), p.148-150

1998

Volltextzugriff (PDF)

Acute relapsing encephalopathy mimicking acute necrotizing encephalopathy in a 4-year-old boy

Brain & development (Tokyo. 1979), 1999-12, Vol.21 (8), p.554-558

1999

Volltextzugriff (PDF)

Elevated serum levels of macrophage colony-stimulating factor in patients with Kawasaki disease complicated by cardiac lesions

Clinical and experimental rheumatology, 2001-11, Vol.19 (6), p.751

2001

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Hypertrophic Cardiomyopathy in Congenital Myotonic Dystrophy

Pediatric neurology, 1998-04, Vol.18 (4), p.366-369

1998

Volltextzugriff (PDF)

Increased serum granulocyte colony-stimulating factor correlates with coronary artery dilatation in Kawasaki disease

European journal of pediatrics, 2002-10, Vol.161 (10), p.538-541

2002

Volltextzugriff (PDF)

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Clinically-oriented monitoring of acute effects of methylphenidate on cerebral hemodynamics in ADHD children using fNIRS

Polyglutamine aggregates stimulate ER stress signals and caspase-12 activation

Blood chimerism in monochorionic twins conceived by induced ovulation: Case report

A complex of synaptic adhesion molecule CADM1, a molecule related to autism spectrum disorder, with MUPP1 in the cerebellum

Effects of high-dose intravenous corticosteroid therapy in Landau-Kleffner syndrome

Acute Infantile Encephalopathy Predominantly Affecting the Frontal Lobes

Clinical features of neonatal toxic shock syndrome-like exanthematous disease emerging in Japan

Two New XPD Patients Compound Heterozygous for the Same Mutation Demonstrate Diverse Clinical Features

Splice site mutation in the hepatocyte nuclear factor-1β gene, IVS2nt + 1G > A, associated with maturity-onset diabetes of the young, renal dysplasia and bicornuate uterus

Effects of dichloroacetate in three patients with MELAS

Efficacy of Iodine-123-15-(p-iodophenyl)-3-R, S-Methylpentadecanoic Acid Single Photon Emission Computed Tomography Imaging in Detecting Myocardial Ischemia in Children With Kawasaki Disease

High serum levels of M‐CSF and G‐CSF in Kawasaki disease

Various types of LRP5 mutations in four patients with osteoporosis-pseudoglioma syndrome: Identification of a 7.2-kb microdeletion using oligonucleotide tiling microarray

Acute disseminated encephalomyelitis after live rubella vaccination

Panipenem-betamipron and decreases in Serum valproic acid concentration

Cost effectiveness of prophylactic treatment with activated prothrombin complex concentrate in a patient with inhibitor-positive hemophilia A

Respiration-deficient cells are caused by a single point mutation in the mitochondrial tRNA-Leu (UUR) gene in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)

Prenatal MRI in a fetus with a giant neck hemangioma: a case report

Mutational analysis of the BMP-1 gene in patients with gastroschisis

Early-Onset Ataxia With Oculomotor Apraxia With a Novel APTX Mutation

Drop episodes in Coffin-Lowry syndrome: exaggerated startle responses treated with clonazepam

Acute relapsing encephalopathy mimicking acute necrotizing encephalopathy in a 4-year-old boy

Elevated serum levels of macrophage colony-stimulating factor in patients with Kawasaki disease complicated by cardiac lesions

Hypertrophic Cardiomyopathy in Congenital Myotonic Dystrophy

Increased serum granulocyte colony-stimulating factor correlates with coronary artery dilatation in Kawasaki disease

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