Published in J Pediatr Hematol Oncol on March 01, 2010
Reduced-dose craniospinal radiotherapy followed by tandem high-dose chemotherapy and autologous stem cell transplantation in patients with high-risk medulloblastoma. Neuro Oncol (2012) 0.91
Institutional experience of paediatric high-grade central nervous system tumours: an analysis of 74 patients and review of the literature. Contemp Oncol (Pozn) (2012) 0.75
High-dose chemotherapy followed by autologous and allogeneic peripheral blood stem cell transplantation for recurrent disseminated trilateral retinoblastoma. Childs Nerv Syst (2011) 0.75
Prognostic factors for the late onset Pompe disease with enzyme replacement therapy: from our experience of 4 cases including an autopsy case. Mol Genet Metab (2010) 2.23
Treatment outcome of medium-dose-rate intracavitary brachytherapy for carcinoma of the uterine cervix: comparison with low-dose-rate intracavitary brachytherapy. Int J Radiat Oncol Biol Phys (2012) 2.00
Mutations in EFHC1 cause juvenile myoclonic epilepsy. Nat Genet (2004) 1.98
Prospective study of high-dose cabergoline treatment of prolactinomas in 150 patients. J Clin Endocrinol Metab (2008) 1.71
Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23. Genet Med (2003) 1.68
Collagen type I alpha2 (COL1A2) is the susceptible gene for intracranial aneurysms. Stroke (2004) 1.68
Phase I/IIa trial of autologous formalin-fixed tumor vaccine concomitant with fractionated radiotherapy for newly diagnosed glioblastoma. Clinical article. J Neurosurg (2011) 1.63
Efficacy of intravenous midazolam for status epilepticus in childhood. Pediatr Neurol (2007) 1.58
Development of hybrid integrated endoscope-holder system for endoscopic microneurosurgery. Neurosurgery (2004) 1.56
Application of nicardipine prolonged-release implants: analysis of 97 consecutive patients with acute subarachnoid hemorrhage. Neurosurgery (2005) 1.56
Individualized high-dose cabergoline therapy for hyperprolactinemic infertility in women with micro- and macroprolactinomas. J Clin Endocrinol Metab (2010) 1.53
Neurofiberscope-guided management of slit-ventricle syndrome due to shunt placement. J Neurosurg (2005) 1.51
Transgenic rescue of hemolytic anemia due to red blood cell pyruvate kinase deficiency. Haematologica (2007) 1.50
Proposed therapeutic strategy for adult low-grade glioma based on aggressive tumor resection. Neurosurg Focus (2015) 1.46
Reduced PLP1 expression in induced pluripotent stem cells derived from a Pelizaeus-Merzbacher disease patient with a partial PLP1 duplication. J Hum Genet (2012) 1.45
A modified Atkins diet is promising as a treatment for glucose transporter type 1 deficiency syndrome. Dev Med Child Neurol (2011) 1.43
Nicardipine prolonged-release implants for preventing cerebral vasospasm after subarachnoid hemorrhage: effect and outcome in the first 100 patients. Neurol Med Chir (Tokyo) (2007) 1.42
Gamma knife surgery for cancer pain-pituitary gland-stalk ablation: a multicenter prospective protocol since 2002. J Neurosurg (2002) 1.41
Progressive visual field defect caused by an unruptured middle cerebral artery aneurysm. Clin Neurol Neurosurg (2013) 1.39
Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness. Ann Neurol (2006) 1.34
Childhood leukemia and magnetic fields in Japan: a case-control study of childhood leukemia and residential power-frequency magnetic fields in Japan. Int J Cancer (2006) 1.33
STXBP1 mutations cause not only Ohtahara syndrome but also West syndrome--result of Japanese cohort study. Epilepsia (2010) 1.30
Endoscopic augmented reality navigation system for endonasal transsphenoidal surgery to treat pituitary tumors: technical note. Neurosurgery (2002) 1.19
Long-term complications after gamma knife surgery for arteriovenous malformations. J Neurosurg (2005) 1.12
Extensive gene deletions in Japanese patients with Diamond-Blackfan anemia. Blood (2012) 1.11
Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort. Adv Neurol (2005) 1.10
Correlation of histology and molecular genetic analysis of 1p, 19q, 10q, TP53, EGFR, CDK4, and CDKN2A in 91 astrocytic and oligodendroglial tumors. Clin Cancer Res (2002) 1.10
Beta-blocker therapy for cardiac dysfunction in patients with muscular dystrophy. Circ J (2006) 1.09
Rasmussen syndrome: multifocal spread of inflammation suggested from MRI and PET findings. Epilepsia (2003) 1.08
Clinical and radiological features related to the growth potential of meningioma. Neurosurg Rev (2006) 1.07
TULIP1 (RALGAPA1) haploinsufficiency with brain development delay. Genomics (2009) 1.06
Bedside monitoring of circulating blood volume after subarachnoid hemorrhage. Stroke (2003) 1.04
Mutational analysis of CACNA1G in idiopathic generalized epilepsy. Mutation in brief #962. Online. Hum Mutat (2007) 1.03
Information-guided surgical management of gliomas using low-field-strength intraoperative MRI. Acta Neurochir Suppl (2011) 1.03
A recurrent KCNT1 mutation in two sporadic cases with malignant migrating partial seizures in infancy. Gene (2013) 1.03
Large facial nerve schwannomas without facial palsy: case reports and review of the literature. Neurosurg Rev (2005) 1.01
DNAJB6 myopathy in an Asian cohort and cytoplasmic/nuclear inclusions. Neuromuscul Disord (2013) 1.00
Expression and quantitative analysis of matrix metalloproteinase-2 and -9 in human gliomas. Brain Tumor Pathol (2004) 0.99
Negative motor seizure arising from the negative motor area: is it ictal apraxia? Epilepsia (2009) 0.98
Role of dual leucine zipper-bearing kinase (DLK/MUK/ZPK) in axonal growth. Neurosci Res (2009) 0.98
Role of p38 mitogen-activated protein kinase on cerebral vasospasm after subarachnoid hemorrhage. Stroke (2004) 0.97
Management and prognosis of cysts developed on long-term follow-up after Gamma Knife radiosurgery for intracranial arteriovenous malformations. Surg Neurol (2007) 0.97
Sulcal pattern and morphology of the superior temporal sulcus. Neuroimage (2004) 0.97
Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression. Blood (2014) 0.96
Myeloid lineage-selective growth of revertant cells in Fanconi anaemia. Br J Haematol (2006) 0.96
CDKL5 alterations lead to early epileptic encephalopathy in both genders. Epilepsia (2011) 0.96
DNA mismatch repair protein (MSH6) correlated with the responses of atypical pituitary adenomas and pituitary carcinomas to temozolomide: the national cooperative study by the Japan Society for Hypothalamic and Pituitary Tumors. J Clin Endocrinol Metab (2013) 0.95
Severe Peters Plus syndrome-like phenotype with anterior eye staphyloma and hypoplastic left heart syndrome: proposal of a new syndrome. Congenit Anom (Kyoto) (2010) 0.95
Phase II clinical study on intraoperative photodynamic therapy with talaporfin sodium and semiconductor laser in patients with malignant brain tumors. J Neurosurg (2013) 0.95
Role of metallothionein in coagulatory disturbance and systemic inflammation induced by lipopolysaccharide in mice. FASEB J (2005) 0.95
Activity of neurons in ventrolateral respiratory groups during swallowing in decerebrate rats. Brain Dev (2003) 0.94
Disappearance of self-mutilating behavior in a patient with lesch-nyhan syndrome after bilateral chronic stimulation of the globus pallidus internus. Case report. J Neurosurg (2003) 0.94
Prediction by FISH analysis of the occurrence of Wilms tumor in aniridia patients. Am J Med Genet (2002) 0.94
MECP2 duplication syndrome in both genders. Brain Dev (2012) 0.94
Agrammatic comprehension caused by a glioma in the left frontal cortex. Brain Lang (2009) 0.93
Successful treatment of a blood blister-like aneurysm of the internal carotid artery by trapping with a high-flow bypass. J Clin Neurosci (2008) 0.92
Antisense PMO found in dystrophic dog model was effective in cells from exon 7-deleted DMD patient. PLoS One (2010) 0.92
A case of metastatic hemangiopericytoma occurring 16 years after initial presentation: with special reference to the clinical behavior and treatment of metastatic hemangiopericytoma. J Nippon Med Sch (2009) 0.91
Benign familial infantile convulsions: linkage to chromosome 16p12-q12 in 14 families. Epilepsia (2004) 0.91
A haplotype spanning two genes, ELN and LIMK1, decreases their transcripts and confers susceptibility to intracranial aneurysms. Hum Mol Genet (2006) 0.91
Anterior interhemispheric approach for 100 tumors in and around the anterior third ventricle. Neurosurgery (2010) 0.91
Radiotherapy with concurrent docetaxel for advanced and recurrent breast cancer. Breast Cancer (2003) 0.91
Association of positional and functional candidate genes FGF1, FBN2, and LOX on 5q31 with intracranial aneurysm. J Hum Genet (2003) 0.90
A novel nonsense mutation with a compound heterozygous mutation in TGFBI gene in lattice corneal dystrophy type I. Jpn J Ophthalmol (2003) 0.90
A functional analysis of GABARAP on 17p13.1 by knockdown zebrafish. J Hum Genet (2010) 0.90
Lesions in the central tegmental tract in autopsy cases of developmental brain disorders. Brain Dev (2010) 0.90
Precise comparison of protoporphyrin IX fluorescence spectra with pathological results for brain tumor tissue identification. Brain Tumor Pathol (2010) 0.90
Discharge diagnoses in infants with apparent life-threatening event. Pediatr Int (2003) 0.90
Adult-onset angiocentric glioma of epithelioid cell-predominant type of the mesial temporal lobe suggestive of a rare but distinct clinicopathological subset within a spectrum of angiocentric cortical ependymal tumors. Neuropathology (2011) 0.90
A modified method to enhance the safety of endoscopic third ventriculostomy (ETV)--transendoscopic pulse-waved microvascular Doppler-assisted ETV, technical note. Childs Nerv Syst (2014) 0.89
A single mutation 202G>A in the human glucose-6-phosphate dehydrogenase gene (G6PD) can cause acute hemolysis by itself. Blood (2002) 0.89
Enhancement of radiosensitivity by dual inhibition of the HER family with ZD1839 ("Iressa") and trastuzumab ("Herceptin"). Int J Radiat Oncol Biol Phys (2006) 0.89
Multivoxel proton MRS for differentiation of radiation-induced necrosis and tumor recurrence after gamma knife radiosurgery for brain metastases. Brain Tumor Pathol (2006) 0.89
Possible role of single-voxel (1)H-MRS in differential diagnosis of suprasellar tumors. J Neurooncol (2008) 0.89
¹H-MRS of intracranial meningiomas: what it can add to known clinical and MRI predictors of the histopathological and biological characteristics of the tumor? Clin Neurol Neurosurg (2010) 0.89
Human eye fields in the frontal lobe as studied by epicortical recording of movement-related cortical potentials. Brain (2004) 0.89
Influence of endothelial nitric oxide synthase T-786C single nucleotide polymorphism on aneurysm size. J Neurosurg (2005) 0.89
Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia. Br J Haematol (2014) 0.88
Mortality in Dravet syndrome: search for risk factors in Japanese patients. Epilepsia (2011) 0.88
Systematic screening of lysyl oxidase-like (LOXL) family genes demonstrates that LOXL2 is a susceptibility gene to intracranial aneurysms. Hum Genet (2007) 0.88
A case-case study of mobile phone use and acoustic neuroma risk in Japan. Bioelectromagnetics (2010) 0.88
Methylation status of the p15 and p16 genes in paediatric myelodysplastic syndrome and juvenile myelomonocytic leukaemia. Br J Haematol (2005) 0.88
Aromatic L-amino acid decarboxylase deficiency associated with epilepsy mimicking non-epileptic involuntary movements. Dev Med Child Neurol (2008) 0.88