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Mutation in Parkinson disease-associated, G-protein-coupled receptor 37 (GPR37/PaelR) is related to autism spectrum disorder

PloS one, 2012-12, Vol.7 (12), p.e51155

2012

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LIN7A depletion disrupts cerebral cortex development, contributing to intellectual disability in 12q21-deletion syndrome

PloS one, 2014-03, Vol.9 (3), p.e92695

2014

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Cadm1-expressing synapses on Purkinje cell dendrites are involved in mouse ultrasonic vocalization activity

PloS one, 2012-01, Vol.7 (1), p.e30151-e30151

2012

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Autism spectrum disorder is related to endoplasmic reticulum stress induced by mutations in the synaptic cell adhesion molecule, CADM1

Cell death & disease, 2010-06, Vol.1 (6), p.e47-e47

2010

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Role of Class III phosphoinositide 3‐kinase in the brain development: possible involvement in specific learning disorders

Journal of neurochemistry, 2016-10, Vol.139 (2), p.245-255

2016

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Role of an adaptor protein Lin‐7B in brain development: possible involvement in autism spectrum disorders

Journal of neurochemistry, 2015-01, Vol.132 (1), p.61-69

2015

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Thoracic duct lymphography by subcutaneous contrast agent injection in a dog with chylothorax

Open veterinary journal (Tripoli, Libya), 2016-01, Vol.6 (3), p.238-241

2016

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Acute neuropharmacological effects of atomoxetine on inhibitory control in ADHD children: a fNIRS study

NeuroImage clinical, 2014-01, Vol.6 (C), p.192-201

2014

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Right prefrontal activation as a neuro-functional biomarker for monitoring acute effects of methylphenidate in ADHD children: An fNIRS study

NeuroImage clinical, 2012-01, Vol.1 (1), p.131-140

2012

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A marked decrease in CD4-positive lymphocytes at the onset of hepatitis in a patient with hepatitis-associated aplastic anemia

Journal of pediatric hematology/oncology, 2012-07, Vol.34 (5), p.375-377

2012

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CASPR2 forms a complex with GPR37 via MUPP1 but not with GPR37(R558Q), an autism spectrum disorder‐related mutation

Journal of neurochemistry, 2015-08, Vol.134 (4), p.783-793

2015

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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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The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysis

Molecular autism, 2015-03, Vol.6 (1), p.17-17, Article 17

2015

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Monitoring of anti-L-asparaginase antibody and L-asparaginase activity levels in a pediatric patient with acute lymphoblastic leukemia and hypersensitivity to native Escherichia coli L-asparaginase during desensitization courses

Journal of pediatric hematology/oncology, 2014-03, Vol.36 (2), p.e91-e93

2014

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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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Mesenteric venous thrombosis in a child with type 2 protein S deficiency

Journal of pediatric hematology/oncology, 2011-03, Vol.33 (2), p.141-143

2011

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Congenital hemophagocytic lymphohistiocytosis in a preterm infant: cytokine profile and a review of the disease

Journal of pediatric hematology/oncology, 2011-07, Vol.33 (5), p.e209-e212

2011

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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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Refractory kaposiform hemangioendothelioma that expressed vascular endothelial growth factor receptor (VEGFR)-2 and VEGFR-3: a case report

Journal of pediatric hematology/oncology, 2009-03, Vol.31 (3), p.194-197

2009

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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

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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

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CASPR 2 forms a complex with GPR 37 via MUPP 1 but not with GPR 37(R558Q), an autism spectrum disorder‐related mutation

Journal of neurochemistry, 2015-08, Vol.134 (4), p.783-793

2015

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Obstructive jaundice as a presentation of ganglioneuroblastoma

Journal of pediatric hematology/oncology, 2005-02, Vol.27 (2), p.112-114

2005

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Prenatal diagnosis of Lowe syndrome by OCRL1 messenger RNA analysis

Prenatal diagnosis, 1999-03, Vol.19 (3), p.269-270

1999

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Follow-up of coronary artery lesions caused by Kawasaki disease and the value of coronary angiography

Chinese medical journal, 2002-05, Vol.115 (5), p.681-684

2002

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Mutation in Parkinson disease-associated, G-protein-coupled receptor 37 (GPR37/PaelR) is related to autism spectrum disorder

LIN7A depletion disrupts cerebral cortex development, contributing to intellectual disability in 12q21-deletion syndrome

Cadm1-expressing synapses on Purkinje cell dendrites are involved in mouse ultrasonic vocalization activity

Autism spectrum disorder is related to endoplasmic reticulum stress induced by mutations in the synaptic cell adhesion molecule, CADM1

Role of Class III phosphoinositide 3‐kinase in the brain development: possible involvement in specific learning disorders

Role of an adaptor protein Lin‐7B in brain development: possible involvement in autism spectrum disorders

Thoracic duct lymphography by subcutaneous contrast agent injection in a dog with chylothorax

Acute neuropharmacological effects of atomoxetine on inhibitory control in ADHD children: a fNIRS study

Right prefrontal activation as a neuro-functional biomarker for monitoring acute effects of methylphenidate in ADHD children: An fNIRS study

A marked decrease in CD4-positive lymphocytes at the onset of hepatitis in a patient with hepatitis-associated aplastic anemia

CASPR2 forms a complex with GPR37 via MUPP1 but not with GPR37(R558Q), an autism spectrum disorder‐related mutation

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

The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysis

Monitoring of anti-L-asparaginase antibody and L-asparaginase activity levels in a pediatric patient with acute lymphoblastic leukemia and hypersensitivity to native Escherichia coli L-asparaginase during desensitization courses

Effects of dichloroacetate in three patients with MELAS

Mesenteric venous thrombosis in a child with type 2 protein S deficiency

Congenital hemophagocytic lymphohistiocytosis in a preterm infant: cytokine profile and a review of the disease

Panipenem-betamipron and decreases in Serum valproic acid concentration

Refractory kaposiform hemangioendothelioma that expressed vascular endothelial growth factor receptor (VEGFR)-2 and VEGFR-3: a case report

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)

CASPR 2 forms a complex with GPR 37 via MUPP 1 but not with GPR 37(R558Q), an autism spectrum disorder‐related mutation

Obstructive jaundice as a presentation of ganglioneuroblastoma

Prenatal diagnosis of Lowe syndrome by OCRL1 messenger RNA analysis

Follow-up of coronary artery lesions caused by Kawasaki disease and the value of coronary angiography

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