Familial medulloblastoma in non-twin siblings

Cellular mechanisms of acute decrease of glutamate release induced by raloxifene in rat cerebral cortex.

Neuropharmacology·2011

Pump efficiency improvement of a C-band tunable fiber laser using optical circulator and tunable fiber gratings.

Applied optics·2007

Cardiotoxicity in imipramine intoxication: report of one case.

Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi·2002

Oral bacterial therapy promotes recovery from acute diarrhea in children.

Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi·2001

Spontaneous closure of ventricular septal defects in the first year of life.

Journal of the Formosan Medical Association = Taiwan yi zhi·2001

Neurologic involvement in an outbreak of enterovirus 71 infection: a hospital-based study.

Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi·2001

Implant design may influence delayed heterotopic ossification after total disk arthroplasty in lumbar spine.

Surgical neurology·2010

A rabbit model for efficacy evaluation of endovascular coil materials.

Surgical neurology·2010

Intracranial angioplasty with Gateway-Wingspan system for symptomatic atherosclerotic stenosis: preliminary results of 27 Chinese patients.

Surgical neurology·2010

Comparison of postoperative cognitive function in patients undergoing surgery for ruptured and unruptured intracranial aneurysm.

Surgical neurology·2010

Neuromodulation of the superior hypogastric plexus: a new option to treat bladder atonia secondary to radical pelvic surgery?

Surgical neurology·2010

Fuzzy Logic in neurosurgery: predicting poor outcomes after lumbar disk surgery in 501 consecutive patients.

Surgical neurology·2010

Integrating transposable elements into blood gene regulatory networks reveals connectivity loss for schizophrenia genes.

The Journal of clinical investigation·2026

T-rex: standardized analysis of germline variants in whole-exome sequencing trios.

Scientific reports·2026

STX1B variant-specific synaptic dysfunction is associated with network hyperexcitability in human iPSC-derived neurons.

EBioMedicine·2026

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

Pharmacology & therapeutics·2026

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

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Familial medulloblastoma in non-twin siblings

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Cellular mechanisms of acute decrease of glutamate release induced by raloxifene in rat cerebral cortex.

Pump efficiency improvement of a C-band tunable fiber laser using optical circulator and tunable fiber gratings.

Cardiotoxicity in imipramine intoxication: report of one case.

Oral bacterial therapy promotes recovery from acute diarrhea in children.

Spontaneous closure of ventricular septal defects in the first year of life.

Neurologic involvement in an outbreak of enterovirus 71 infection: a hospital-based study.

Implant design may influence delayed heterotopic ossification after total disk arthroplasty in lumbar spine.

A rabbit model for efficacy evaluation of endovascular coil materials.

Intracranial angioplasty with Gateway-Wingspan system for symptomatic atherosclerotic stenosis: preliminary results of 27 Chinese patients.

Comparison of postoperative cognitive function in patients undergoing surgery for ruptured and unruptured intracranial aneurysm.

Neuromodulation of the superior hypogastric plexus: a new option to treat bladder atonia secondary to radical pelvic surgery?

Fuzzy Logic in neurosurgery: predicting poor outcomes after lumbar disk surgery in 501 consecutive patients.

Integrating transposable elements into blood gene regulatory networks reveals connectivity loss for schizophrenia genes.

T-rex: standardized analysis of germline variants in whole-exome sequencing trios.

STX1B variant-specific synaptic dysfunction is associated with network hyperexcitability in human iPSC-derived neurons.

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

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Familial medulloblastoma in non-twin siblings

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