Eiichiro Uyama, MD - Related publications

Affiliations: 
Neurology Kumamoto University, Kumamoto-shi, Kumamoto-ken, Japan 
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50 most relevant papers in past 60 days:
Year Citation  Score
2020 Davies M, Dodd S, Coultate M, Ross A, Pears G, Gnaneswaran B, Tzivinikos C, Konidari A, Cheng J, Auth MK, Cameron F, Tamhne S, Renji E, Nair M, Baillie C, et al. From Paris to Montreal: disease regression is common during long term follow-up of paediatric Crohn's disease. Scandinavian Journal of Gastroenterology. 1-6. PMID 31928099 DOI: 10.1080/00365521.2019.1710765   
2020 Molenaar JP, Verhoeven JI, Rodenburg RJ, Kamsteeg EJ, Erasmus CE, Vicart S, Behin A, Bassez G, Magot A, Péréon Y, Brandom BW, Guglielmi V, Vattemi G, Chevessier F, Mathieu J, et al. Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients. Brain : a Journal of Neurology. 143: 452-466. PMID 32040565 DOI: 10.1093/brain/awz410   
2020 Zhang MQ, Wang XH, Chen YL, Zhao KL, Cai YQ, An CL, Lin MG, Mu XD. [Clinical features of 2019 novel coronavirus pneumonia in the early stage from a fever clinic in Beijing]. Zhonghua Jie He He Hu Xi Za Zhi = Zhonghua Jiehe He Huxi Zazhi = Chinese Journal of Tuberculosis and Respiratory Diseases. 43: E013. PMID 32061066 DOI: 10.3760/cma.j.issn.1001-0939.2020.0013   
2020 He J, Zhou WJ, Shi J, Lin JL, Zhang BQ, Sun ZH. [Analysis of genotypes, EEG and phenotypes of tuberous sclerosis complex patients]. Zhonghua Yi Xue Za Zhi. 100: 136-140. PMID 31937054 DOI: 10.3760/cma.j.issn.0376-2491.2020.02.011   
2020 Salvati M, Bruzzaniti P, Relucenti M, Nizzola M, Familiari P, Giugliano M, Scafa AK, Galletta S, Li X, Chen R, Barbaranelli C, Frati A, Santoro A. Retrospective and Randomized Analysis of Influence and Correlation of Clinical and Molecular Prognostic Factors in a Mono-Operative Series of 122 Patients with Glioblastoma Treated with STR or GTR. Brain Sciences. 10. PMID 32050461 DOI: 10.3390/brainsci10020091   
2020 Wang Y, Wang O, Nie M, Li Y, Jiang Y, Li M, Xia W, Xing X. CLINICAL AND GENETIC FINDINGS IN A CHINESE COHORT OF PATIENTS WITH DIGEORGE SYNDROME-RELATED HYPOPARATHYROIDISM. Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists. PMID 32045288 DOI: 10.4158/EP-2019-0498   
2020 Campagnolo M, Taioli F, Cacciavillani M, Ruiz M, Luigetti M, Salvalaggio A, Castellani F, Testi S, Ferrarini M, Cavallaro T, Gasparotti R, Fabrizi GM, Briani C. Sporadic hereditary neuropathies misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy: Pitfalls and red flags. Journal of the Peripheral Nervous System : Jpns. PMID 31919945 DOI: 10.1111/jns.12362   
2020 Desgrouas C, Varlet AA, Dutour A, Galant D, Merono F, Bonello-Palot N, Bourgeois P, Lasbleiz A, Petitjean C, Ancel P, Levy N, Badens C, Gaborit B. Unraveling Mutations in Metabolic Syndrome: Cellular Phenotype and Clinical Pitfalls. Cells. 9. PMID 32012908 DOI: 10.3390/cells9020310   
2020 Aguirre F, Villa AM. [Myasthenia gravis. Register of 190 cases in a single center]. Medicina. 80: 10-16. PMID 32044736   
2020 Nagappa M, Sharma S, Govindaraj P, Chickabasaviah YT, Siram R, Shroti A, Debnath M, Sinha S, Bindu PS, Taly AB. PMP22 Gene-Associated Neuropathies: Phenotypic Spectrum in a Cohort from India. Journal of Molecular Neuroscience : Mn. PMID 31993930 DOI: 10.1007/s12031-020-01488-w   
2020 Németh T, Pécsy B, Géczi T, Sas K, Szpisjak L, Rieth A, Kiss V, Szőnyegi F, Tiszlavicz L, Zombori T, Lázár G, Furák J. [Successful multidisciplinary management of tetraplegia with a thoracic operation. ]. Orvosi Hetilap. 161: 33-38. PMID 31884815 DOI: 10.1556/650.2020.31560   
2020 Liu XX, Zhang S, Liu N, Sun AP, Zhang YS, Fan DS. [The diagnostic value of tremor analysis for defining the Parkinson's disease subtype]. Zhonghua Yi Xue Za Zhi. 100: 207-212. PMID 32008288 DOI: 10.3760/cma.j.issn.0376-2491.2020.03.010   
2020 Panneman DM, Wortmann SB, Haaxma CA, van Hasselt PM, Wolf NI, Hendriks Y, Küsters B, van Emst-de Vries S, van de Westerlo E, Koopman WJH, Wintjes L, van den Brandt F, de Vries M, Lefeber DJ, Smeitink JAM, et al. Variants in NGLY1 lead to intellectual disability, myoclonus epilepsy, sensorimotor axonal polyneuropathy and mitochondrial dysfunction. Clinical Genetics. PMID 31957011 DOI: 10.1111/cge.13706   
2020 Xie W, Xu J, Hu S, Li S, Wang W, Cameron Yin C, Toruner G, Tang Z, Jeffrey Medeiros L, Tang G. iAMP21 in acute myeloid leukemia is associated with complex karyotype, TP53 mutation and dismal outcome. Modern Pathology : An Official Journal of the United States and Canadian Academy of Pathology, Inc. PMID 32034282 DOI: 10.1038/s41379-020-0494-3   
2020 Zhong L, Wang J, Wang W, Wang L, Quan M, Tang X, Gou L, Wei M, Xiao J, Zhang T, Sui R, Zhou Q, Song H. Juvenile Onset Splenomegaly and Oculopathy Due to Germline Mutation in ALPK1. Journal of Clinical Immunology. PMID 31939038 DOI: 10.1007/s10875-020-00741-6   
2020 Yazılıtaş F, Kargın Çakıcı E, Kurt Şükür ED, Can G, Güngör T, Orhan D, Bülbül M. C3 glomerulopathy: experience of a pediatric nephrology center. Acta Clinica Belgica. 1-5. PMID 31914901 DOI: 10.1080/17843286.2020.1713450   
2020 Yazılıtaş F, Kargın Çakıcı E, Kurt Şükür ED, Can G, Güngör T, Orhan D, Bülbül M. C3 glomerulopathy: experience of a pediatric nephrology center. Acta Clinica Belgica. 1-5. PMID 31914901 DOI: 10.1080/17843286.2020.1713450   
2020 Ahmed P, Chaudhry QUN, Satti TM, Mahmood SK, Ghafoor T, Shahbaz N, Khan MA, Satti HS, Akram Z, Iftikhar R. Epidemiology of aplastic anemia: a study of 1324 cases. Hematology (Amsterdam, Netherlands). 25: 48-54. PMID 31906834 DOI: 10.1080/16078454.2019.1711344   
2020 Martinson HA, Mallari D, Richter C, Wu TT, Tiesinga J, Alberts SR, Olnes MJ. Molecular Classification of Gastric Cancer among Alaska Native People. Cancers. 12. PMID 31941061 DOI: 10.3390/cancers12010198   
2020 Ehmke N, Cusmano-Ozog K, Koenig R, Holtgrewe M, Nur B, Mihci E, Babcock H, Gonzaga-Jauregui C, Overton JD, Xiao J, Martinez A, Muenke M, Balzer A, Jochim J, El Choubassi N, et al. Biallelic variants in KYNU cause a multisystemic syndrome with hand hyperphalangism. Bone. 115219. PMID 31923704 DOI: 10.1016/j.bone.2019.115219   
2020 Jiangyi W, Gang G, Guohai S, Dingwei Y. Germline mutation of TSC1 or TSC2 gene in Chinese patients with bilateral renal angiomyolipomas and mutation spectrum of Chinese TSC patients. Aging. 12. PMID 31927531 DOI: 10.18632/aging.102654   
2020 Sun Y, Zhao M, Lao IW, Yu L, Wang J. The clinicopathological spectrum of pseudomyogenic hemangioendothelioma: report of an additional series with review of the literature. Virchows Archiv : An International Journal of Pathology. PMID 31980959 DOI: 10.1007/s00428-020-02753-4   
2020 Abu-Ghname A, Perdanasari AT, Raj S, Seema J, Wilson KD, Maricevich RS. Access to Multidisciplinary Care for Patients With 22q11.2 Deletion Syndrome: Identifying Breakdowns in the Screening Process. The Journal of Craniofacial Surgery. PMID 31917711 DOI: 10.1097/SCS.0000000000006142   
2020 Liao Y, Tian Y, Ye R, Tang C, Tang Q, Ma F, Yang S, He H, Zhong D. Risk and treatment of symptomatic epidural hematoma after anterior cervical spine surgery: A retrospective clinical study. Medicine. 99: e18711. PMID 31914081 DOI: 10.1097/MD.0000000000018711   
2020 Sasatani Y, Okauchi S, Ohara G, Kagohashi K, Satoh H. Long-term maintenance of nutritional status with ninjinyoueito in terminal patients with chronic respiratory disease: Two case reports. Biomedical Reports. 12: 121-124. PMID 32042420 DOI: 10.3892/br.2019.1267   
2020 Bai SL, Wang JY, Zhou YQ, Yu DS, Gao XM, Li LL, Yang F. [Analysis of the first cluster of cases in a family of novel coronavirus pneumonia in Gansu Province]. Zhonghua Yu Fang Yi Xue Za Zhi [Chinese Journal of Preventive Medicine]. 54: E005. PMID 32064855 DOI: 10.3760/cma.j.issn.0253-9624.2020.0005   
2020 Marsili L, Overwater E, Hanna N, Baujat G, Baars MJH, Boileau C, Bonneau D, Brehin AC, Capri Y, Cheung HY, Dulfer E, Gerard M, Gouya L, Hilhorst-Hofstee Y, Houweling AC, et al. Phenotypic spectrum of TGFB3 disease-causing variants in a Dutch-French cohort and first report of a homozygous patient. Clinical Genetics. PMID 31898322 DOI: 10.1111/cge.13700   
2020 Bhakuni T, Sharma A, Biswas A, Bano S, Mahapatra M, Saxena R, Jairajpuri MA. Identification and characterization of a novel variant in C-terminal region of Antithrombin (Ala427Thr) associated with type II AT deficiency leading to polymer formation. Journal of Thrombosis and Thrombolysis. PMID 32020514 DOI: 10.1007/s11239-020-02048-0   
2020 Marashi Nia SF, Aghaie Meybodi M, Sutton R, Bansal A, Olyaee M, Hejazi R. Outcome, complication and follow-up of patients with esophageal foreign body impaction: an academic institute's 15 years of experience. Diseases of the Esophagus : Official Journal of the International Society For Diseases of the Esophagus. PMID 32052054 DOI: 10.1093/dote/doz103   
2020 Salim F, Khan F, Nasir M, Ali R, Iqbal A, Raza A. Frequency of Intraoperative Hypotension After the Induction of Anesthesia in Hypertensive Patients with Preoperative Angiotensin-converting Enzyme Inhibitors. Cureus. 12: e6614. PMID 32064194 DOI: 10.7759/cureus.6614   
2020 Bose G, Freedman MS. Precision medicine in the multiple sclerosis clinic: Selecting the right patient for the right treatment. Multiple Sclerosis (Houndmills, Basingstoke, England). 1352458519887324. PMID 31965903 DOI: 10.1177/1352458519887324   
2020 Untas A, Vioulac C, Boujut E, Delannoy C, Poivret D, Rat AC, Beauvais C, Giraudet Le Quintrec JS. What Is Relatives' Role in Arthritis Management? A Qualitative Study of the Perceptions of Patient-Relative Dyads. Patient Preference and Adherence. 14: 45-53. PMID 32021116 DOI: 10.2147/PPA.S231919   
2020 Liu M, He P, Liu HG, Wang XJ, Li FJ, Chen S, Lin J, Chen P, Liu JH, Li CH. [Clinical characteristics of 30 medical workers infected with new coronavirus pneumonia]. Zhonghua Jie He He Hu Xi Za Zhi = Zhonghua Jiehe He Huxi Zazhi = Chinese Journal of Tuberculosis and Respiratory Diseases. 43: E016. PMID 32062957 DOI: 10.3760/cma.j.issn.1001-0939.2020.0016   
2020 Glyn TC, Ho MW, Lambert AP, Thomas JDJ, Douek IF, Andrews RC, King RJ. Patients with morbid obesity should not be routinely screened for Cushing's syndrome: Results of retrospective study of patients attending a specialist weight management service. Clinical Obesity. e12358. PMID 31994330 DOI: 10.1111/cob.12358   
2020 Rosa Neto NS, Bento JCB, Pereira RMR. Depression, sleep disturbances, pain, disability and quality of LIFE in Brazilian Fabry disease patients. Molecular Genetics and Metabolism Reports. 22: 100547. PMID 31871893 DOI: 10.1016/j.ymgmr.2019.100547   
2020 Kahraman BO, Savci S, Ozsoy I, Baran A, Acar S, Ozpelit E, Balci A, Sevinc C, Akdeniz B. Effects of neuromuscular electrical stimulation in patients with pulmonary arterial hypertension: a randomized controlled pilot study. Journal of Cardiology. PMID 32001075 DOI: 10.1016/j.jjcc.2019.12.013   
2020 Kohn M, Karras A, Zaidan M, Bénière C, de Fréminville JB, Laribi K, Perrin MC, Malphettes M, Le Calloch R, Anglaret B, Martiniuc J, Bailly S, Chevret S, Molina T, Thervet E, et al. Lymphomas with kidney involvement: the French multicenter retrospective LyKID study. Leukemia & Lymphoma. 1-9. PMID 32037948 DOI: 10.1080/10428194.2019.1697811   
2020 Sharmin M, Chowdhury AM, Ali MA, Rahman MW, Hossain MA, Rahman MH, Sharmin P, Roy AS, Chowdhury B. Clinical Profile and Immediate Outcome of Children Admitted With Acute Glomerulonephritis in Pediatrics Department of A Tertiary Level Hospital. Mymensingh Medical Journal : Mmj. 29: 5-15. PMID 31915329   
2020 Gaut D, Burkenroad A, Duong T, Feammelli J, Sasine J, Schiller G. Venetoclax combination therapy in relapsed/refractory acute myeloid leukemia: A single institution experience. Leukemia Research. 90: 106314. PMID 32035355 DOI: 10.1016/j.leukres.2020.106314   
2020 Lee Y, Park S, Lee JS, Kim SY, Cho J, Yoo Y, Lee S, Yoo T, Lee M, Seo J, Lee J, Kneissl J, Lee J, Jeon H, Jeon EY, et al. Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population. Scientific Reports. 10: 1413. PMID 31996704 DOI: 10.1038/s41598-020-58101-8   
2020 Nikhanj A, Yogasundaram H, Miskew Nichols B, Richman-Eisenstat J, Phan C, Bakal JA, Siddiqi ZA, Oudit GY. Cardiac Intervention Improves Heart Disease and Clinical Outcomes in Patients With Muscular Dystrophy in a Multidisciplinary Care Setting. Journal of the American Heart Association. 9: e014004. PMID 31931688 DOI: 10.1161/JAHA.119.014004   
2020 Abdu L, Bawahab N, Mohammed Hussain RW, Qary H, Saeedi A, Alhibshi N. Prevalence and Treatment Outcome of Nasolacrimal Duct Obstruction in Saudi Children with Down Syndrome. Cureus. 12: e6672. PMID 31976186 DOI: 10.7759/cureus.6672   
2020 Aparicio T, Henriques J, Manfredi S, Tougeron D, Bouché O, Pezet D, Piessen G, Coriat R, Zaanan A, Legoux JL, Terrebone E, Pocard M, Gornet JM, Lecomte T, Lombard-Bohas C, ... , et al. Small bowel adenocarcinoma: Results from a nationwide prospective ARCAD-NADEGE cohort study of 347 patients. International Journal of Cancer. PMID 31912484 DOI: 10.1002/ijc.32860   
2020 Takahashi MP, Yamamoto R, Kubota T, Matsuura T, Ishigaki K, Sunada Y, Komaki H, Takada H, Kuru S, Matsumura T. [Study of care practices for patients with myotonic dystrophy in Japan-Nationwide patient survey]. Rinsho Shinkeigaku = Clinical Neurology. PMID 31956156 DOI: 10.5692/clinicalneurol.cn-001349   
2020 Elsayed HH, Soliman S, Hamed AM, El-Saqqa A, Hussein AT, BinMelhi E, Nassar WAM. Venous pectoralis minor syndrome: a rare subdivision of the thoracic outlet syndrome. Interactive Cardiovascular and Thoracic Surgery. 30: 33-35. PMID 31873744 DOI: 10.1093/icvts/ivz212   
2020 Moutinho-Ribeiro P, Costa-Moreira P, Adem B, Batista I, Almeida M, Barroca H, Lopes J, Carneiro F, Melo SA, Macedo G. Exosomal glypican-1 for risk stratification of pancreatic cystic lesions: A case of pathological progression in the absence of any suspicious imaging finding. Pancreatology : Official Journal of the International Association of Pancreatology (Iap) ... [Et Al.]. PMID 32024605 DOI: 10.1016/j.pan.2020.01.015   
2020 Chen H, Zhang Q, Chen R, Yuan X, Lin X, Yang X, Zhang Y. Lipoid Congenital Adrenal Hyperplasia due to Steroid Acute Regulatory Protein (STAR) Variants in Three Chinese Patients. The Journal of Steroid Biochemistry and Molecular Biology. 105635. PMID 32068072 DOI: 10.1016/j.jsbmb.2020.105635   
2020 Du MY, Xu M, Deng J, Liu L, Guo T, Xia LH, Hu Y, Mei H. Evaluation of different scoring systems and gene mutations for the prognosis of myelodysplastic syndrome (MDS) in Chinese population. Journal of Cancer. 11: 508-519. PMID 31897246 DOI: 10.7150/jca.30363   
2020 Tang Y, Li J, Xie N, Yang X, Liu L, Wu H, Tian C, He Y, Wang X, He Q, Hu ZY, Ouyang Q. gene mutations in the helical domain correlate with high tumor mutation burden and poor prognosis in metastatic breast carcinomas with late-line therapies. Aging. 12. PMID 31980592 DOI: 10.18632/aging.102701   
2020 Juven A, Nambot S, Piton A, Jean-Marçais N, Masurel A, Callier P, Marle N, Mosca-Boidron AL, Kuentz P, Philippe C, Chevarin M, Duffourd Y, Gautier E, Munnich A, Rio M, et al. Primrose syndrome: a phenotypic comparison of patients with a ZBTB20 missense variant versus a 3q13.31 microdeletion including ZBTB20. European Journal of Human Genetics : Ejhg. PMID 32071410 DOI: 10.1038/s41431-020-0582-3