Senda Ajroud-Driss - Related publications

Affiliations: 
Neurology Northwestern University, Evanston, IL 
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50 most relevant papers in past 60 days:
Year Citation  Score
2020 Kotan D, Özözen Ayas Z, Tunca C, Gungen BD, Akçimen F, Başak AN. Phenotypic and genotypic features of patients diagnosed with ALS in the city of Sakarya, Turkey. Acta Neurologica Belgica. PMID 32671691 DOI: 10.1007/s13760-020-01441-z   
2020 Lin J, Chen W, Huang P, Xie Y, Zheng M, Yao X. The distinct manifestation of young-onset amyotrophic lateral sclerosis in China. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-8. PMID 32729724 DOI: 10.1080/21678421.2020.1797091   
2020 Mueller C, Berry JD, McKenna-Yasek DM, Gernoux G, Owegi MA, Pothier LM, Douthwright CL, Gelevski D, Luppino SD, Blackwood M, Wightman NS, Oakley DH, Frosch MP, Flotte TR, Cudkowicz ME, et al. Suppression with Adeno-Associated Virus and MicroRNA in Familial ALS. The New England Journal of Medicine. 383: 151-158. PMID 32640133 DOI: 10.1056/NEJMoa2005056   
2020 Martínez de LaPiscina I, Hernández-Ramírez LC, Portillo N, Gómez-Gila AL, Urrutia I, Martínez-Salazar R, García-Castaño A, Aguayo A, Rica I, Gaztambide S, Faucz FR, Keil MF, Lodish MB, Quezado M, Pankratz N, et al. Rare Germline Variants in Pediatric Patients With Cushing's Disease: What Is Their Role? Frontiers in Endocrinology. 11: 433. PMID 32714280 DOI: 10.3389/fendo.2020.00433   
2020 Molnár MJ, Borsos B, Várdi KV, Grosz Z, Sebők Á, Dézsi L, Almássy Z, Kerényi L, Jobbágy Z, Jávor L, Bidló J. [The long-term follow-up of enzyme replacement treatment in late onset Pompe disease]. Ideggyogyaszati Szemle. 73: 151-159. PMID 32579304 DOI: 10.18071/isz.73.0151   
2020 McClatchey MA, du Toit ZD, Vaughan R, Whatley SD, Martins S, Hegde S, Naude JTW, Thomas DH, Griffiths DF, Research Consortium GE, Clarke AJ, Fry AE. Focal segmental glomerulosclerosis and mild intellectual disability in a patient with a novel de novo truncating TRIM8 mutation. European Journal of Medical Genetics. 103972. PMID 32531461 DOI: 10.1016/j.ejmg.2020.103972   
2020 Oliveira Santos M, Gromicho M, Pinto S, De Carvalho M. Clinical characteristics in young-adult ALS - results from a Portuguese cohort study. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-4. PMID 32654518 DOI: 10.1080/21678421.2020.1790611   
2020 Lim SH, Kim JH, Han KH, Ahn YH, Kang HG, Ha IS, Cheong HI. Genotype and Phenotype Analyses in Pediatric Patients with Mutations. Journal of Clinical Medicine. 9. PMID 32708349 DOI: 10.3390/jcm9072320   
2020 Okada T, Washida K, Irie K, Saito S, Noguchi M, Tomita T, Koga M, Toyoda K, Okazaki S, Koizumi T, Mizuta I, Mizuno T, Ihara M. Prevalence and Atypical Clinical Characteristics of Mutations Among Patients Admitted for Acute Lacunar Infarctions. Frontiers in Aging Neuroscience. 12: 130. PMID 32477100 DOI: 10.3389/fnagi.2020.00130   
2020 Dumic KK, Anticevic D, Petrinovic-Doresic J, Zigman T, Zarković K, Rokic F, Vugrek O. Lowe syndrome - Old and new evidence of secondary mitochondrial dysfunction. European Journal of Medical Genetics. 104022. PMID 32712215 DOI: 10.1016/j.ejmg.2020.104022   
2020 Chen SJ, Lee BC, Lee NC, Chien YH, Hwu WL, Lin CH. Clinical, radiological, and genetic characteristics in patients with Huntington's disease in a Taiwanese cohort. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 32643304 DOI: 10.1002/ajmg.b.32810   
2020 Lu Y, Sun K, Guo S, Wang J, Li A, Rong X, Wang T, Shang Y, Chang W, Wang S. Early Warning Indicators of Severe COVID-19: A Single-Center Study of Cases From Shanghai, China. Frontiers in Medicine. 7: 432. PMID 32766268 DOI: 10.3389/fmed.2020.00432   
2020 Zhao J, Gao HY, Feng ZY, Wu QJ. A Retrospective Analysis of the Clinical and Epidemiological Characteristics of COVID-19 Patients in Henan Provincial People's Hospital, Zhengzhou, China. Frontiers in Medicine. 7: 286. PMID 32582740 DOI: 10.3389/fmed.2020.00286   
2020 Park E, Lee C, Kim NKD, Ahn YH, Park YS, Lee JH, Kim SH, Cho MH, Cho H, Yoo KH, Shin JI, Kang HG, Ha IS, Park WY, Cheong HI. Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis. Journal of Clinical Medicine. 9. PMID 32604935 DOI: 10.3390/jcm9062013   
2020 Ohno S, Ozawa J, Fukuyama M, Makiyama T, Horie M. An NGS-based genotyping in LQTS; minor genes are no longer minor. Journal of Human Genetics. PMID 32681117 DOI: 10.1038/s10038-020-0805-z   
2020 Zhang LL, Cao XX, Shen KN, Han HX, Zhang CL, Qiu Y, Zhao H, Gao XM, Feng J, Zhang L, Zhou DB, Li J. Clinical characteristics and treatment outcome of type I cryoglobulinemia in Chinese patients: a single-center study of 45 patients. Annals of Hematology. PMID 32535708 DOI: 10.1007/s00277-020-04123-1   
2020 Deng X, Liu B, Li J, Zhang J, Zhao Y, Xu K. Blood biochemical characteristics of patients with coronavirus disease 2019 (COVID-19): a systemic review and meta-analysis. Clinical Chemistry and Laboratory Medicine. PMID 32554832 DOI: 10.1515/cclm-2020-0338   
2020 Malek E, Ismail H, Doumiati H, Salameh J. Characteristics of amyotrophic lateral sclerosis in Lebanon-a chart review. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-6. PMID 32633637 DOI: 10.1080/21678421.2020.1788095   
2020 Kurucu N, Akyüz C, Varan A, Akçören Z, Aydin B, Yalçin B, Kutluk T. Primary Paraspinal and Spinal Epidural Non-Hodgkin Lymphoma in Childhood. Journal of Pediatric Hematology/Oncology. PMID 32520843 DOI: 10.1097/MPH.0000000000001858   
2020 Wang H, Bing D, Li J, Xie L, Xiong F, Lan L, Wang D, Guan J, Wang Q. High Frequency of Variants and Phenotype Progression of Auditory Neuropathy in a Chinese Population. Neural Plasticity. 2020: 5625768. PMID 32684920 DOI: 10.1155/2020/5625768   
2020 Blincoe A, Heeg M, Campbell PK, Hines M, Khojah A, Klein-Gitelman M, Talano JA, Speckmann C, Touzot F, Lankester A, Legger GE, Rivière JG, Garcia-Prat M, Alonso L, Putti MC, et al. Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic Lymphohistiocytosis. Journal of Clinical Immunology. PMID 32638196 DOI: 10.1007/s10875-020-00814-6   
2020 Rahmani F, Rayzan E, Rahmani MR, Shahkarami S, Zoghi S, Rezaei A, Aryan Z, Najafi M, Rohlfs M, Jeske T, Aflatoonian M, Chavoshzadeh Z, Farahmand F, Motamed F, Rohani P, et al. Clinical and Mutation Description of the First Iranian Cohort of Infantile Inflammatory Bowel Disease: The Iranian Primary Immunodeficiency Registry (IPIDR). Immunological Investigations. 1-15. PMID 32633164 DOI: 10.1080/08820139.2020.1776725   
2020 Sánchez-Valle J, Tejero H, Fernández JM, Juan D, Urda-García B, Capella-Gutiérrez S, Al-Shahrour F, Tabarés-Seisdedos R, Baudot A, Pancaldi V, Valencia A. Interpreting molecular similarity between patients as a determinant of disease comorbidity relationships. Nature Communications. 11: 2854. PMID 32504002 DOI: 10.1038/s41467-020-16540-x   
2020 Turan H, Dağdeviren Çakır A, Özer Y, Tarçın G, Özcabi B, Ceylaner S, Ercan O, Evliyaoğlu SO. Clinical and genetic characteristics of patients with corticosterone methyloxidase deficiency type 2: Novel mutations in . Journal of Clinical Research in Pediatric Endocrinology. PMID 32539318 DOI: 10.4274/jcrpe.galenos.2020.2019.0216   
2020 Aardoom MA, Kemos P, Tindemans I, Aloi M, Koletzko S, Levine A, Turner D, Veereman G, Neyt M, Russell RK, Walters TD, Ruemmele FM, Samsom JN, Croft NM, de Ridder L, , et al. International prospective observational study investigating the disease course and heterogeneity of paediatric-onset inflammatory bowel disease: the protocol of the PIBD-SETQuality inception cohort study. Bmj Open. 10: e035538. PMID 32611739 DOI: 10.1136/bmjopen-2019-035538   
2020 Serratrice C, Stirnemann J, Berrahal A, Belmatoug N, Camou F, Caillaud C, Billette de Villemeur T, Dalbies F, Cador B, Froissart R, Masseau A, Brassier A, Hivert B, Swiader L, Bertchansky I, et al. A Cross-Sectional Retrospective Study of Non-Splenectomized and Never-Treated Patients with Type 1 Gaucher Disease. Journal of Clinical Medicine. 9. PMID 32708003 DOI: 10.3390/jcm9082343   
2020 Sha Y, Wei X, Ding L, Ji Z, Mei L, Huang X, Su Z, Wang W, Zhang X, Lin S. Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotype. Journal of Human Genetics. PMID 32555313 DOI: 10.1038/s10038-020-0790-2   
2020 Samukawa M, Nakamura N, Hirano M, Morikawa M, Sakata H, Nishino I, Izumi R, Suzuki N, Kuroda H, Shiga K, Saigoh K, Aoki M, Kusunoki S. Neutral Lipid Storage Disease Associated with the PNPLA2 Gene: Case Report and Literature Review. European Neurology. 1-6. PMID 32564019 DOI: 10.1159/000508346   
2020 Chen Y, Huang H, He Y, Chen M, Seidler U, Tian D, Xiao F. A20 Haploinsufficiency in a Chinese Patient With Intestinal Behcet's Disease-Like Symptoms: A Case Report. Frontiers in Immunology. 11: 1414. PMID 32719680 DOI: 10.3389/fimmu.2020.01414   
2020 Soveizi M, Mahdieh N, Setoodeh A, Sayarifard F, Abbasi F, Bose HS, Rabbani B, Rabbani A. p.Gln318X and p.Val281Leu as the Major Variants of Gene in Children with Idiopathic Premature Pubarche. International Journal of Endocrinology. 2020: 4329791. PMID 32714392 DOI: 10.1155/2020/4329791   
2020 Matesanz SE, Curry C, Gross B, Rubin AI, Linn R, Yum SW, Kichula EA. Clinical Course in a Patient With Spinal Muscular Atrophy Type 0 Treated With Nusinersen and Onasemnogene Abeparvovec. Journal of Child Neurology. 883073820928784. PMID 32515646 DOI: 10.1177/0883073820928784   
2020 Siranosian JJ, Nery FC, Alves CRR, Siranosian BA, Lyons NJ, Eichelberger EJ, Garner R, Da Silva Duarte Lepez S, Johnstone AJ, Subramanian A, Swoboda KJ. Whole-blood dysregulation of actin-cytoskeleton pathway in adult spinal muscular atrophy patients. Annals of Clinical and Translational Neurology. PMID 32558393 DOI: 10.1002/acn3.51092   
2020 Kim CY, Wirth T, Hubsch C, Németh AH, Okur V, Anheim M, Drouot N, Tranchant C, Rudolf G, Chelly J, Tatton-Brown K, Blauwendraat C, Vonsattel JPG, Cortes E, Alcalay RN, et al. Early-onset parkinsonism is a manifestation of the PPP2R5D p.E200K mutation. Annals of Neurology. PMID 32743835 DOI: 10.1002/ana.25863   
2020 Vera G, Sorlin A, Delplancq G, Lecoquierre F, Brasseur-Daudruy M, Petit F, Smol T, Ziegler A, Bonneau D, Colin E, Mercier S, Cogné B, Bézieau S, Edery P, Lesca G, et al. Clinical and molecular description of 19 patients with GATAD2B-Associated Neurodevelopmental Disorder (GAND). European Journal of Medical Genetics. 104004. PMID 32688057 DOI: 10.1016/j.ejmg.2020.104004   
2020 Dabas G, Mahajan R, De D, Handa S, Kumar R, Dayal D, Suthar R, Panigrahi I. Managing syndromic congenital ichthyosis at a tertiary care institute - Genotype-phenotype correlations, and novel treatments. Dermatologic Therapy. e13816. PMID 32533806 DOI: 10.1111/dth.13816   
2020 Bey AL, Gorman MP, Gallentine W, Kohlenberg TM, Frankovich J, Jiang YH, Van Haren K. Subacute Neuropsychiatric Syndrome in Girls With Mutations Responds to Immunomodulation. Pediatrics. 145. PMID 32015180 DOI: 10.1542/peds.2019-1490   
2020 Pytte J, Flynn LL, Anderton RS, Mastaglia FL, Theunissen F, James I, Pfaff A, Koks S, Saunders AM, Bedlack R, Burns DK, Lutz MW, Siddique N, Siddique T, Roses AD, et al. Disease-modifying effects of an structural variant in a predominantly ALS cohort. Neurology. Genetics. 6: e470. PMID 32754644 DOI: 10.1212/NXG.0000000000000470   
2020 Hassan K, Sher G, Hamid E, Hazima KA, Abdelrahman H, Al Mudahka F, Al-Masri W, Sankar J, Daryaee M, Shawish R, Khan MA, Nawaz Z. Outcome associated with EPCAM founder mutation c.499dup in Qatar. European Journal of Medical Genetics. 104023. PMID 32735948 DOI: 10.1016/j.ejmg.2020.104023   
2020 Hassan K, Sher G, Hamid E, Hazima KA, Abdelrahman H, Al Mudahka F, Al-Masri W, Sankar J, Daryaee M, Shawish R, Khan MA, Nawaz Z. Outcome associated with EPCAM founder mutation c.499dup in Qatar. European Journal of Medical Genetics. 104023. PMID 32735948 DOI: 10.1016/j.ejmg.2020.104023   
2020 Hassan K, Sher G, Hamid E, Hazima KA, Abdelrahman H, Al Mudahka F, Al-Masri W, Sankar J, Daryaee M, Shawish R, Khan MA, Nawaz Z. Outcome associated with EPCAM founder mutation c.499dup in Qatar. European Journal of Medical Genetics. 104023. PMID 32735948 DOI: 10.1016/j.ejmg.2020.104023   
2020 Tian S, Chang Z, Wang Y, Wu M, Zhang W, Zhou G, Zou X, Tian H, Xiao T, Xing J, Chen J, Han J, Ning K, Wu T. Clinical Characteristics and Reasons for Differences in Duration From Symptom Onset to Release From Quarantine Among Patients With COVID-19 in Liaocheng, China. Frontiers in Medicine. 7: 210. PMID 32574322 DOI: 10.3389/fmed.2020.00210   
2020 Zhang B, Zhou X, Zhu C, Song Y, Feng F, Qiu Y, Feng J, Jia Q, Song Q, Zhu B, Wang J. Immune Phenotyping Based on the Neutrophil-to-Lymphocyte Ratio and IgG Level Predicts Disease Severity and Outcome for Patients With COVID-19. Frontiers in Molecular Biosciences. 7: 157. PMID 32719810 DOI: 10.3389/fmolb.2020.00157   
2020 Deng J, Wu X, Ling Y, Liu X, Zheng X, Ye W, Yuping G. The prognostic impact of variant allele frequency (VAF) in TP53 mutant patients with MDS: a systematic review and meta-analysis. European Journal of Haematology. PMID 32621334 DOI: 10.1111/ejh.13483   
2020 Linzmeyer GFA, Miyake FK, Santos TAFCGD, Skare TL. Serum immunoglobulin a deficiency and autoimmune comorbidities: a crossectional study in 281 patients with systemic lupus erythematosus. Revista Da Associacao Medica Brasileira (1992). 66: 752-756. PMID 32696881 DOI: 10.1590/1806-9282.66.6.752   
2020 Haug N, Deischinger C, Gyimesi M, Kautzky-Willer A, Thurner S, Klimek P. High-risk multimorbidity patterns on the road to cardiovascular mortality. Bmc Medicine. 18: 44. PMID 32151252 DOI: 10.1186/s12916-020-1508-1   
2020 Rentas S, Pillai V, Wertheim GB, Akgumus GT, Nichols KE, Deardorff MA, Conlin LK, Li MM, Olson TS, Luo M. Evolution of histomorphologic, cytogenetic, and genetic abnormalities in an untreated patient with MIRAGE syndrome. Cancer Genetics. 245: 42-48. PMID 32619790 DOI: 10.1016/j.cancergen.2020.06.002   
2020 Rentas S, Pillai V, Wertheim GB, Akgumus GT, Nichols KE, Deardorff MA, Conlin LK, Li MM, Olson TS, Luo M. Evolution of histomorphologic, cytogenetic, and genetic abnormalities in an untreated patient with MIRAGE syndrome. Cancer Genetics. 245: 42-48. PMID 32619790 DOI: 10.1016/j.cancergen.2020.06.002   
2020 Rentas S, Pillai V, Wertheim GB, Akgumus GT, Nichols KE, Deardorff MA, Conlin LK, Li MM, Olson TS, Luo M. Evolution of histomorphologic, cytogenetic, and genetic abnormalities in an untreated patient with MIRAGE syndrome. Cancer Genetics. 245: 42-48. PMID 32619790 DOI: 10.1016/j.cancergen.2020.06.002   
2020 Srivastava SK, Marathe N, Raj A, Bhosale S, Dhole K. Surgical Management of Hirayama Disease: A Rare Entity with Unusual Clinical Features. Asian Journal of Neurosurgery. 15: 405-408. PMID 32656141 DOI: 10.4103/ajns.AJNS_291_19   
2020 Van Es MA, Van Eijk RPA, Bunte TM, Van Den Berg LH. A placebo-controlled trial to investigate the safety and efficacy of Penicillin G/Hydrocortisone in patients with ALS (PHALS trial). Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-9. PMID 32627599 DOI: 10.1080/21678421.2020.1788093