PubRank

Takao Takahashi

Author PubWeight™ 155.54‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Clinical and biological features associated with epidermal growth factor receptor gene mutations in lung cancers. J Natl Cancer Inst 2005 13.00
2 Thrombopoietin/MPL signaling regulates hematopoietic stem cell quiescence and interaction with the osteoblastic niche. Cell Stem Cell 2007 4.31
3 Somatic mutations of the HER2 kinase domain in lung adenocarcinomas. Cancer Res 2005 4.25
4 Novel mutation of human DNA polymerase gamma associated with mitochondrial toxicity induced by anti-HIV treatment. J Infect Dis 2007 1.85
5 Methylation and gene silencing of the Ras-related GTPase gene in lung and breast cancers. Ann Surg Oncol 2006 1.79
6 Allelic and non-allelic heterogeneities in pyridoxine dependent seizures revealed by ALDH7A1 mutational analysis. Mol Genet Metab 2007 1.75
7 The RNA-binding protein HuD regulates neuronal cell identity and maturation. Proc Natl Acad Sci U S A 2005 1.66
8 Efficacy of intravenous midazolam for status epilepticus in childhood. Pediatr Neurol 2007 1.58
9 Polymorphisms, mutations, and amplification of the EGFR gene in non-small cell lung cancers. PLoS Med 2007 1.52
10 Hypoxic regulation of the cerebral microcirculation is mediated by a carbon monoxide-sensitive hydrogen sulfide pathway. Proc Natl Acad Sci U S A 2012 1.50
11 GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling. Proc Natl Acad Sci U S A 2009 1.47
12 Complete mutation analysis panel of the 39 human HOX genes. Teratology 2002 1.47
13 Phenotypic spectrum of CHARGE syndrome with CHD7 mutations. J Pediatr 2006 1.45
14 Retracted Methylation of apoptosis related genes in the pathogenesis and prognosis of prostate cancer. Cancer Lett 2006 1.40
15 Aberrant methylation of trail decoy receptor genes is frequent in multiple tumor types. Int J Cancer 2004 1.32
16 Cell-autonomous roles of ARX in cell proliferation and neuronal migration during corticogenesis. J Neurosci 2008 1.28
17 Retracted Aberrant methylation profile of human malignant mesotheliomas and its relationship to SV40 infection. Oncogene 2005 1.25
18 Efficacy and immunologic responses to influenza vaccine in HIV-1-infected patients. J Acquir Immune Defic Syndr 2005 1.22
19 Aberrant methylation of HIN-1 (high in normal-1) is a frequent event in many human malignancies. Int J Cancer 2005 1.21
20 Retracted Aberrant methylation of heparan sulfate glucosamine 3-O-sulfotransferase 2 genes as a biomarker in colorectal cancer. Anticancer Res 2010 1.18
21 Very low pandemic influenza A (H1N1) 2009 mortality associated with early neuraminidase inhibitor treatment in Japan: analysis of 1000 hospitalized children. J Infect 2011 1.17
22 Large fontanelles are a shared feature of haploinsufficiency of RUNX2 and its co-activator CBFB. Congenit Anom (Kyoto) 2004 1.12
23 Size distribution of retrovirally marked lineages matches prediction from population measurements of cell cycle behavior. J Neurosci Res 2002 1.08
24 Absent inner dynein arms in a fetus with familial hydrocephalus-situs abnormality. Am J Med Genet A 2004 1.08
25 Small heat shock protein 27 mutation in a Japanese patient with distal hereditary motor neuropathy. J Hum Genet 2005 1.05
26 Efficacy, safety, and pharmacokinetics of intravenous peramivir in children with 2009 pandemic H1N1 influenza A virus infection. Antimicrob Agents Chemother 2011 1.02
27 Altered patterns of neuron production in the p27 knockout mouse. Dev Neurosci 2005 1.02
28 Position-specific expression of Hox genes along the gastrointestinal tract. Congenit Anom (Kyoto) 2004 1.02
29 A case of esophageal adenocarcinoma arising from the ectopic gastric mucosa in the thoracic esophagus. Rare Tumors 2010 1.00
30 Protein-losing enteropathy caused by gastrointestinal tract-involved Langerhans cell histiocytosis. Pediatrics 2010 0.99
31 The roles of surgical oncologists in the new era: minimally invasive surgery for early gastric cancer and adjuvant surgery for metastatic gastric cancer. Pathobiology 2011 0.99
32 Molecular pathology of Shprintzen-Goldberg syndrome. Am J Med Genet A 2006 0.99
33 Retracted Aberrant methylation of Reprimo in lung cancer. Lung Cancer 2005 0.97
34 Genetic regulation of proliferation/differentiation characteristics of neural progenitor cells in the developing neocortex. Brain Dev 2009 0.96
35 Severe congenital lipodystrophy and a progeroid appearance: Mutation in the penultimate exon of FBN1 causing a recognizable phenotype. Am J Med Genet A 2013 0.95
36 Population dynamics during cell proliferation and neuronogenesis in the developing murine neocortex. Results Probl Cell Differ 2002 0.95
37 Presence of simian virus 40 DNA sequences in human lymphoid and hematopoietic malignancies and their relationship to aberrant promoter methylation of multiple genes. Cancer Res 2004 0.95
38 Embryonic expression profile of chicken CHD7, the ortholog of the causative gene for CHARGE syndrome. Birth Defects Res A Clin Mol Teratol 2007 0.94
39 Differential methylation of genes that regulate cytokine signaling in lymphoid and hematopoietic tumors. Oncogene 2005 0.93
40 Elevated urine pregnanetriolone definitively establishes the diagnosis of classical 21-hydroxylase deficiency in term and preterm neonates. J Clin Endocrinol Metab 2004 0.93
41 Clinical significance of aggressive hepatectomy for colorectal liver metastasis, evaluated from the HGF/c-Met pathway. Int J Oncol 2010 0.92
42 The utility of vitamin K3 (menadione) against pancreatic cancer. Anticancer Res 2008 0.92
43 Functional hemispheric specialization in processing phonemic and prosodic auditory changes in neonates. Front Psychol 2011 0.91
44 Microduplication of Xq24 and Hartsfield syndrome with holoprosencephaly, ectrodactyly, and clefting. Am J Med Genet A 2012 0.91
45 Genetic analysis of essential cardiac transcription factors in 256 patients with non-syndromic congenital heart defects. Circ J 2012 0.91
46 An Alu retrotransposition-mediated deletion of CHD7 in a patient with CHARGE syndrome. Am J Med Genet A 2007 0.90
47 A false positive for metastatic lymph nodes in the axillary region of a breast cancer patient following mastectomy. Breast Cancer 2009 0.90
48 Biweekly docetaxel, cisplatin, and 5-fluorouracil (DCF) chemotherapy for advanced esophageal squamous cell carcinoma: a phase I dose-escalation study. Cancer Chemother Pharmacol 2010 0.90
49 Reference values for urinary steroids in Japanese newborn infants: gas chromatography/mass spectrometry in selected ion monitoring. Endocr J 2003 0.90
50 Microdeletion of the Down syndrome critical region at 21q22. Am J Med Genet A 2010 0.90
51 Expression of vascular endothelial growth factor receptors is closely related to the histological grade of hepatocellular carcinoma. Oncol Rep 2006 0.89
52 Cleidocranial dysplasia plus vascular anomalies with 6p21.2 microdeletion spanning RUNX2 and VEGF. Am J Med Genet A 2006 0.88
53 Effects of methylenetetrahydrofolate reductase and reduced folate carrier 1 polymorphisms on high-dose methotrexate-induced toxicities in children with acute lymphoblastic leukemia or lymphoma. J Pediatr Hematol Oncol 2006 0.88
54 Pathways to acute humoral rejection. Am J Pathol 2004 0.87
55 Gene knock-outs of inositol 1,4,5-trisphosphate receptors types 1 and 2 result in perturbation of cardiogenesis. PLoS One 2010 0.87
56 Extracellular signal-regulated kinase phosphorylation due to menadione-induced arylation mediates growth inhibition of pancreas cancer cells. Cancer Chemother Pharmacol 2007 0.87
57 Differences in voriconazole trough plasma concentrations per oral dosages between children younger and older than 3 years of age. Pediatr Blood Cancer 2010 0.86
58 1p34.3 deletion involving GRIK3: Further clinical implication of GRIK family glutamate receptors in the pathogenesis of developmental delay. Am J Med Genet A 2013 0.86
59 Reconstitution activity of hypoxic cultured human cord blood CD34-positive cells in NOG mice. Biochem Biophys Res Commun 2008 0.86
60 Effect of hepatocyte growth factor on progression of liver metastasis in colorectal cancer. Hepatogastroenterology 2010 0.86
61 Micropenis and the 5alpha-reductase-2 (SRD5A2) gene: mutation and V89L polymorphism analysis in 81 Japanese patients. J Clin Endocrinol Metab 2003 0.86
62 Safety and efficacy of linezolid in 16 infants and children in Japan. J Infect Chemother 2012 0.86
63 Oncologic outcomes of laparoscopic gastrectomy: a single-center safety and feasibility study. Surg Endosc 2013 0.86
64 A major influence of CYP2C19 genotype on the steady-state concentration of N-desmethylclobazam. Brain Dev 2004 0.85
65 Screening for Alagille syndrome mutations in the JAG1 and NOTCH2 genes using denaturing high-performance liquid chromatography. Genet Test 2007 0.85
66 Characterization of the aryl hydrocarbon receptor repressor gene and association of its Pro185Ala polymorphism with micropenis. Teratology 2002 0.85
67 Interstitial microdeletion of 4p16.3: contribution of WHSC1 haploinsufficiency to the pathogenesis of developmental delay in Wolf-Hirschhorn syndrome. Am J Med Genet A 2010 0.85
68 Challenge for a better combination with basic evidence. Int J Clin Oncol 2008 0.85
69 Improvement of adherence to guidelines for antiemetic medication enhances emetic control in patients with colorectal cancer receiving chemotherapy of moderate emetic risk. Anticancer Res 2013 0.84
70 Docetaxel, nedaplatin, and S-1 (DGS) chemotherapy for advanced esophageal carcinoma: a phase I dose-escalation study. Anticancer Res 2011 0.84
71 Involvement of insulin-like growth factor-I and insulin-like growth factor binding proteins in pro-B-cell development. Exp Hematol 2006 0.84
72 Infectious and inflammatory disorders of the circulatory system and stroke in childhood. Curr Opin Neurol 2002 0.83
73 Case report: Adult phenotype of Mulvihill-Smith syndrome. Am J Med Genet A 2009 0.83
74 Influence of MTHFR and RFC1 polymorphisms on toxicities during maintenance chemotherapy for childhood acute lymphoblastic leukemia or lymphoma. J Pediatr Hematol Oncol 2008 0.83
75 Evaluation of treatment for synchronous hepatic metastases from gastric cancer with special reference to long-term survivors. Surg Today 2002 0.83
76 Rapamycin enhances chemotherapy-induced cytotoxicity by inhibiting the expressions of TS and ERK in gastric cancer cells. Int J Cancer 2010 0.83
77 Persistent hypertension despite successful dilation of a stenotic renal artery in a boy with neurofibromatosis type 1. Am J Med Genet A 2013 0.82
78 Immunohistochemical study of claudin 18 involvement in intestinal differentiation during the progression of intraductal papillary mucinous neoplasm. Anticancer Res 2010 0.82
79 EFNB1 mutation at the ephrin ligand-receptor dimerization interface in a patient with craniofrontonasal syndrome. Congenit Anom (Kyoto) 2007 0.82
80 A novel mtDNA C11777A mutation in Leigh syndrome. Mitochondrion 2003 0.82
81 Antigen-specific T-cell responses in patients with non-IgE-mediated gastrointestinal food allergy are predominantly skewed to T(H)2. J Allergy Clin Immunol 2012 0.82
82 Critical role of c-Met and Ki67 in progress of biliary carcinoma. Am Surg 2010 0.82
83 ST2 requires Th2-, but not Th17-, type airway inflammation in epicutaneously antigen- sensitized mice. Allergol Int 2012 0.82
84 Klebsiella oxytoca-positive, penicillin-associated hemorrhagic enterocolitis in children. Pediatr Int 2010 0.82
85 Eosinophilic cystitis presented as a manifestation of hypereosinophilic syndrome: a case report and review of the literature. Nephron Extra 2013 0.82
86 Cerebellar long-term depression requires dephosphorylation of TARP in Purkinje cells. Eur J Neurosci 2012 0.82
87 Laparoscopic technique and safety experience with barbed suture closure for pelvic cavity after abdominoperineal resection. World J Surg Oncol 2013 0.82
88 Upper airway obstruction in neonates and infants with CHARGE syndrome. Am J Med Genet A 2007 0.81
89 Congenital corneal staphyloma as a complication of Kabuki syndrome. Am J Med Genet A 2012 0.81
90 Novel real-time PCR assay using a universal molecular marker for diagnosis of hematologic cancers. Int J Cancer 2005 0.81
91 Clinical evaluation of modified reconstruction method after pancreatoduodenectomy. Hepatogastroenterology 2009 0.81
92 Screening for partial deletions in the CREBBP gene in Rubinstein-Taybi syndrome patients using multiplex PCR/liquid chromatography. Genet Test 2006 0.81
93 Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood: trisomy 9 mosaicism. Congenit Anom (Kyoto) 2006 0.81
94 12q14 microdeletion syndrome and short stature with or without relative macrocephaly. Am J Med Genet A 2012 0.81
95 Branchial arch defects and 19p13.12 microdeletion: defining the critical region into a 0.8 M base interval. Am J Med Genet A 2011 0.81
96 Split hand foot malformation with whorl-like pigmentary pattern: phenotypic expression of somatic mosaicism for the p63 mutation. Am J Med Genet A 2008 0.81
97 Effective and safe immunizations with live-attenuated vaccines for children after living donor liver transplantation. Vaccine 2008 0.80
98 Strategy for synchronous and multiple liver metastasis. Hepatogastroenterology 2012 0.80
99 Histopathological and behavioral improvement of murine mucopolysaccharidosis type VII by intracerebral transplantation of neural stem cells. Mol Ther 2005 0.80
100 The cross-sectional head circumference growth curves for Japanese from birth to 18 years of age: the 1990 and 1992-1994 national survey data. Ann Hum Biol 2002 0.80
101 Inositol 1,4,5-trisphosphate receptors are essential for the development of the second heart field. J Mol Cell Cardiol 2011 0.80
102 A Phase II Study of Third-Line Combination Chemotherapy with Bevacizumab Plus S-1 for Metastatic Colorectal Cancer with Mutated KRAS (SAVIOR Study). Oncology 2016 0.80
103 Concurrent deletion of BMP4 and OTX2 genes, two master genes in ophthalmogenesis. Eur J Med Genet 2012 0.80
104 BiClamp forceps significantly shorten the operation time for breast surgery. Surg Today 2010 0.79
105 Contribution of thymidylate synthase to gemcitabine therapy for advanced pancreatic cancer. Pancreas 2010 0.79
106 Comprehensive screening of the thiopurine methyltransferase polymorphisms by denaturing high-performance liquid chromatography. Genet Test 2005 0.79
107 Multiple café au lait spots in familial patients with MAP2K2 mutation. Am J Med Genet A 2013 0.79
108 Multiplex PCR/liquid chromatography assay for screening of subtelomeric rearrangements. Genet Test 2007 0.79
109 Cholesterol granuloma in the pancreas accompanied by peritoneal disseminated lesions. Pancreas 2011 0.79
110 A case report on efficacy of Abound™ for anti-EGFR antibody-associated skin disorder in metastatic colon cancer. World J Surg Oncol 2014 0.79
111 Deficiency of BLNK hampers PLC-gamma2 phosphorylation and Ca2+ influx induced by the pre-B-cell receptor in human pre-B cells. Immunology 2004 0.79
112 In utero exposure to dioxin causes neocortical dysgenesis through the actions of p27Kip1. Proc Natl Acad Sci U S A 2010 0.79
113 Age-dependent change in behavioral feature in Rubinstein-Taybi syndrome. Congenit Anom (Kyoto) 2012 0.79
114 Hypoglycemia associated with L-asparaginase in acute lymphoblastic leukemia treatment: a case report. Exp Hematol Oncol 2012 0.79
115 Activity-dependent regulation of HCN1 protein in cortical neurons. Biochem Biophys Res Commun 2009 0.79
116 Combination therapy of 5-fluorouracil with rapamycin for hormone receptor-negative human breast cancer. Anticancer Res 2010 0.79
117 Mechanisms underlying early development of pulmonary vascular obstructive disease in Down syndrome: An imbalance in biosynthesis of thromboxane A2 and prostacyclin. Am J Med Genet A 2010 0.79
118 Mucinous cystic neoplasm of the pancreas in a male patient. Rare Tumors 2011 0.79
119 Long-term outcomes of treatment of gastric gastrointestinal stromal tumor by laparoscopic surgery: review of the literature and our experience. Hepatogastroenterology 2014 0.78
120 Effectiveness of lidocaine infusion for status epilepticus in childhood: a retrospective multi-institutional study in Japan. Brain Dev 2008 0.78
121 Partial deletion of LIS1: a pitfall in molecular diagnosis of Miller-Dieker syndrome. Pediatr Neurol 2007 0.78
122 Effects of sedative and nonsedative antihistamines on prefrontal activity during verbal fluency task in young children: a near-infrared spectroscopy (NIRS) study. Psychopharmacology (Berl) 2009 0.78
123 Postexposure prophylaxis for influenza in pediatric wards oseltamivir or zanamivir after rapid antigen detection. Pediatr Infect Dis J 2012 0.78
124 Diagnosis of Russell-Silver syndrome by the combined bisulfite restriction analysis-denaturing high-performance liquid chromatography assay. Genet Test Mol Biomarkers 2009 0.78
125 Molecular targets for cancer therapy and prevention. Chest 2004 0.78
126 [Evaluation of the efforts of pharmaceutical care services before medical examination at an outpatient cancer chemotherapy clinic]. Gan To Kagaku Ryoho 2013 0.78
127 Acquisition of G₀ state by CD34-positive cord blood cells after bone marrow transplantation. Exp Hematol 2010 0.78
128 A single case of single-port access laparoscopic appendectomy during the puerperium. Int Surg 2015 0.78
129 Trivalent inactivated influenza vaccine effective against influenza A(H3N2) variant viruses in children during the 2014/15 season, Japan. Euro Surveill 2016 0.78
130 Tissue-limited ring chromosome 18 mosaicism as a cause of Pitt-Hopkins syndrome. Am J Med Genet A 2012 0.77
131 Identification of a prosencephalic-specific enhancer of SALL1: comparative genomic approach using the chick embryo. Pediatr Res 2007 0.77
132 Interleukin-7 contributes to human pro-B-cell development in a mouse stromal cell-dependent culture system. Exp Hematol 2007 0.77
133 Screening for CHARGE syndrome mutations in the CHD7 gene using denaturing high-performance liquid chromatography. Genet Test 2006 0.77
134 Association between patient age at the time of surgical treatment for endometriosis and aryl hydrocarbon receptor repressor polymorphism. Fertil Steril 2009 0.77
135 Growth-chart-based qualitative evaluation of height growth after hematopoietic stem cell transplantation. Pediatr Transplant 2006 0.77
136 Severe craniosynostosis with Noonan syndrome phenotype associated with SHOC2 mutation: clinical evidence of crosslink between FGFR and RAS signaling pathways. Am J Med Genet A 2014 0.77
137 Two distinctive classic genetic syndromes, 22q11.2 deletion syndrome and Angelman syndrome, occurring within the same family. Am J Med Genet A 2009 0.77
138 FOLFIRI plus bevacizumab as a first-line treatment for Japanese patients with metastatic colorectal cancer: a JACCRO CC-03 multicenter phase II study. Cancer Chemother Pharmacol 2013 0.77
139 Comprehensive screening of CREB-binding protein gene mutations among patients with Rubinstein-Taybi syndrome using denaturing high-performance liquid chromatography. Congenit Anom (Kyoto) 2005 0.76
140 Iridic and retinal coloboma associated with prenatal methimazole exposure. Am J Med Genet A 2005 0.76
141 Evaluation of efficacy and safety of generic levofolinate in patients who received colorectal cancer chemotherapy. Med Oncol 2010 0.76
142 Colocolic intussusception associated with pneumatosis cystoides intestinalis after cord blood stem cell transplantation. J Pediatr Gastroenterol Nutr 2004 0.76
143 Multiple polypoid masses in the gastrointestinal tract in patient with Menkes disease on copper-histidinate therapy. Eur J Pediatr 2004 0.76
144 Caudal regression and tracheoesophageal malformation induced by adriamycin: a novel chick model of VATER association. Pediatr Res 2009 0.76
145 Antihistamine effects on prefrontal cortex activity during working memory process in preschool children: a near-infrared spectroscopy (NIRS) study. Neurosci Res 2010 0.76
146 Retrospective evaluation of the clinical necessity of external biliary drainage after pancreaticoduodenectomy. Hepatogastroenterology 2014 0.76
147 Hydrocephalus with Hirschsprung disease: severe end of X-linked hydrocephalus spectrum. Am J Med Genet A 2012 0.76
148 A case report of papilla Vater carcinoma showing positive expression of thymidine phosphorylase. Hepatogastroenterology 2004 0.76
149 Porencephaly in a fetus and HANAC in her father: variable expression of COL4A1 mutation. Am J Med Genet A 2014 0.76
150 Surgical Indications for Multiple and Synchronous Liver Metastases from Colorectal Cancer. Hepatogastroenterology 2014 0.76
151 Neocentromere marker chromosome of distal 3q mimicking dup(3q) syndrome phenotype. Am J Med Genet A 2008 0.76
152 Gallbladder adenocarcinoma with extended intramural spread in adenomyomatosis of the gallbladder with the pearl necklace sign. Am Surg 2011 0.76
153 Successful surgical resection for peritoneal implantation of hepatocellular carcinoma at the paracardial portion. J Oncol 2009 0.75
154 A case delayed hemorrhage from the stump of the superior rectal artery after abdominoperineal resection of the rectum. Case Rep Med 2010 0.75
155 Genome-wide screening of dioxin-responsive genes in fetal brain: bioinformatic and experimental approaches. Congenit Anom (Kyoto) 2006 0.75
156 Determining timing of hepatectomy for colorectal cancer with distant metastasis according to imaging-based tumor shrinkage ratio. Int J Med Sci 2013 0.75
157 Cryptococcal meningitis in an immunocompetent child. Eur J Pediatr 2005 0.75
158 A 38-year-old man with pulmonary hypertension, who had undergone atrial septal closure 26 years previously. Keio J Med 2003 0.75
159 [To take the initiative as the distinguished professional leaders]. No To Hattatsu 2014 0.75
160 [Advances in neuroscience and therapeutic research on neurological diseases--the present status and future prospects (discussion)]. Brain Nerve 2007 0.75
161 [Effect of post-exposure prophylaxis with oseltamivir for those in contacts with influenza patients in pediatric wards]. Kansenshogaku Zasshi 2004 0.75
162 The effect of p53 gene expression on the inhibition of cell proliferation by paclitaxel. Cancer Chemother Pharmacol 2007 0.75
163 Two distinctive mechanisms leading to disruption of the SHOX transcription unit in a single family. Am J Med Genet A 2007 0.75
164 Posterior cerebral artery dissection on a serial magnetic resonance angiography. Brain Dev 2011 0.75
165 [Roundtable discussion: advances in neuroscience and therapeutic research on neurological diseases--the present status and future prospects]. No To Shinkei 2007 0.75
166 Clinical utility of an array comparative genomic hybridization analysis for Williams syndrome. Congenit Anom (Kyoto) 2014 0.75
167 Severe obstructive sleep apnea in Loeys-Dietz syndrome successfully treated using continuous positive airway pressure. Am J Med Genet A 2013 0.75
168 Daytime somnolence in an adult with Smith-Magenis syndrome. Am J Med Genet A 2013 0.75
169 [ATTEMPTS TO INCREASE SURGEON'S MOTIVATION IN A REMOTE AND SMALL HOSPITAL]. Nihon Geka Gakkai Zasshi 2015 0.75
170 [Treatment of advanced gastric cancer in the elderly]. Nihon Geka Gakkai Zasshi 2012 0.75
171 [Neocortical histogenesis and intractable epilepsy]. No To Hattatsu 2014 0.75
172 [How to facilitate transition from child-oriented to adult-oriented care]. Nihon Rinsho 2010 0.75
173 Transverse limb defect in a patient with Jacobsen syndrome: concurrence of malformation and disruption. Am J Med Genet A 2010 0.75
174 Catastrophic autonomic crisis with cardiovascular collapse in spinal muscular atrophy with respiratory distress type 1. J Child Neurol 2012 0.75
175 Axillary ultrasound examination is useful for selecting patients optimally suited for sentinel lymph node biopsy after primary systemic chemotherapy. Am J Surg 2012 0.75
176 A case of nonalcoholic and juvenile pancreatic ductal stones to evaluate the most favorable strategy for pancreatic ductal stones. Am Surg 2010 0.75
177 [The 9th international conference of the asian clinical oncology society in Japan after a twenty year interval--what is the standpoint of Japan in Asia ?]. Gan To Kagaku Ryoho 2011 0.75
178 Status epilepticus. Handb Clin Neurol 2013 0.75
179 Pharmacists contribute to the improved efficiency of medical practices in the outpatient cancer chemotherapy clinic. J Eval Clin Pract 2011 0.75
180 [Sentinel lymph node biopsy under local anaesthesia for outpatient]. Nihon Rinsho 2012 0.75
181 [To assume leadership far and wide]. No To Hattatsu 2015 0.75
182 Retraction: DNA methylation profiles of lymphoid and hematopoietic malignancies. Clin Cancer Res 2012 0.75
183 Reversible diffuse white matter lesion in Alagille syndrome. Pediatr Neurol 2011 0.75
184 Hyperinsulinemic hypoglycemia in a newborn infant with trisomy 13. Am J Med Genet A 2004 0.75
185 Establishment of a novel childhood acute myeloid leukaemia cell line, KOPM-88, containing partial tandem duplication of the MLL gene and an in vivo model for childhood acute myeloid leukaemia using NOD/SCID mice. Br J Haematol 2007 0.75
186 [Relationship between the Incidence of Hypomagnesemia and Acneiform Rash and the Therapeutic Effect of Anti-EGFR Monoclonal Antibody in Patients with Metastatic Colorectal Cancer]. Gan To Kagaku Ryoho 2016 0.75