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For: Pearson TS, Pons R, Ghaoui R, Sue CM. Genetic mimics of cerebral palsy. Mov Disord 2019;34:625-36. [PMID: 30913345 DOI: 10.1002/mds.27655] [Cited by in Crossref: 29] [Cited by in F6Publishing: 22] [Article Influence: 9.7] [Reference Citation Analysis]
Number Citing Articles
1 Rosello M, Caro-llopis A, Orellana C, Oltra S, Alemany-albert M, Marco-hernandez AV, Monfort S, Pedrola L, Martinez F, Tomás M. Hidden etiology of cerebral palsy: genetic and clinical heterogeneity and efficient diagnosis by next-generation sequencing. Pediatr Res 2021;90:284-8. [DOI: 10.1038/s41390-020-01250-3] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Aravamuthan BR, Fehlings D, Shetty S, Fahey M, Gilbert L, Tilton A, Kruer MC. Variability in Cerebral Palsy Diagnosis. Pediatrics 2021;147:e2020010066. [PMID: 33402528 DOI: 10.1542/peds.2020-010066] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Saputra L, Kumar KR. Challenges and Controversies in the Genetic Diagnosis of Hereditary Spastic Paraplegia. Curr Neurol Neurosci Rep 2021;21:15. [PMID: 33646413 DOI: 10.1007/s11910-021-01099-x] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
4 Bastos PAD, Barbosa R. A Newly Identified Int22h1/Int22h2‐Mediated Xq28 Duplication Syndrome Case Misdiagnosed as Cerebral Palsy. Journal of Pediatric Neurology. [DOI: 10.1055/s-0042-1743435] [Reference Citation Analysis]
5 Prasad N, Gottlich C, Nhan D, Hamosh A, Sponseller PD. Orthopaedic Problems in 35 Patients With Organic Acid Disorders. J Pediatr Orthop 2021;41:e457-63. [PMID: 34096551 DOI: 10.1097/BPO.0000000000001812] [Reference Citation Analysis]
6 McGovern E, Pringsheim T, Medina A, Cosentino C, Shalash A, Sardar Z, Fung VSC, Kurian MA, Roze E; MDS Task Force on Pediatrics. Transitional Care for Young People with Neurological Disorders: A Scoping Review with A Focus on Patients with Movement Disorders. Mov Disord 2021;36:1316-24. [PMID: 33200525 DOI: 10.1002/mds.28381] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Saberian S, Rowan P, Hammes F, Patel P, Fernandez-cortes F, de Zarate IBO, Buesch K. Burden of illness of aromatic L-amino acid decarboxylase deficiency: a survey of physicians in southern Europe. Current Medical Research and Opinion. [DOI: 10.1080/03007995.2022.2078097] [Reference Citation Analysis]
8 Michelson DJ, Clark RD. Optimizing Genetic Diagnosis of Neurodevelopmental Disorders in the Clinical Setting. Clin Lab Med 2020;40:231-56. [PMID: 32718497 DOI: 10.1016/j.cll.2020.05.001] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
9 Ebrahimi-Fakhari D, Saffari A, Pearl PL. Childhood-onset hereditary spastic paraplegia and its treatable mimics. Mol Genet Metab 2021:S1096-7192(21)00735-6. [PMID: 34183250 DOI: 10.1016/j.ymgme.2021.06.006] [Reference Citation Analysis]
10 Smith SE, Gannotti M, Hurvitz EA, Jensen FE, Krach LE, Kruer MC, Msall ME, Noritz G, Rajan DS, Aravamuthan BR. Adults with Cerebral Palsy Require Ongoing Neurologic Care: A Systematic Review. Ann Neurol 2021;89:860-71. [PMID: 33550625 DOI: 10.1002/ana.26040] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
11 Sadowska M, Sarecka-Hujar B, Kopyta I. Cerebral Palsy: Current Opinions on Definition, Epidemiology, Risk Factors, Classification and Treatment Options. Neuropsychiatr Dis Treat 2020;16:1505-18. [PMID: 32606703 DOI: 10.2147/NDT.S235165] [Cited by in Crossref: 43] [Cited by in F6Publishing: 24] [Article Influence: 21.5] [Reference Citation Analysis]
12 Suchowersky O, Ashtiani S, Au PB, McLeod S, Estiar MA, Gan-Or Z, Rouleau GA. Hereditary spastic paraplegia initially diagnosed as cerebral palsy. Clin Park Relat Disord 2021;5:100114. [PMID: 34816117 DOI: 10.1016/j.prdoa.2021.100114] [Reference Citation Analysis]
13 Lu B, Zeng F, Xing W, Liang L, Huo J, Tan C, Zhu L, Liu Z. Decreased mitochondrial DNA copy number in children with cerebral palsy quantified by droplet digital PCR. Clinica Chimica Acta 2020;503:122-7. [DOI: 10.1016/j.cca.2020.01.018] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
14 Indelicato E, Zech M, Amprosi M, Boesch S. Untangling neurodevelopmental disorders in the adulthood: a movement disorder is the clue. Orphanet J Rare Dis 2022;17:55. [PMID: 35172867 DOI: 10.1186/s13023-022-02218-8] [Reference Citation Analysis]
15 Martinez-Ramirez D, Walker RH, Rodríguez-Violante M, Gatto EM; Rare Movement Disorders Study Group of International Parkinson’s Disease. Review of Hereditary and Acquired Rare Choreas. Tremor Other Hyperkinet Mov (N Y) 2020;10:24. [PMID: 32832197 DOI: 10.5334/tohm.548] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
16 Hakami WS, Hundallah KJ, Tabarki BM. Metabolic and genetic disorders mimicking cerebral palsy. Neurosciences (Riyadh) 2019;24:155-63. [PMID: 31380813 DOI: 10.17712/nsj.2019.3. 20190045] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
17 Horber V, Grasshoff U, Sellier E, Arnaud C, Krägeloh-Mann I, Himmelmann K. The Role of Neuroimaging and Genetic Analysis in the Diagnosis of Children With Cerebral Palsy. Front Neurol 2020;11:628075. [PMID: 33633660 DOI: 10.3389/fneur.2020.628075] [Reference Citation Analysis]
18 Friedman JM, van Essen P, van Karnebeek CDM. Cerebral palsy and related neuromotor disorders: Overview of genetic and genomic studies. Mol Genet Metab 2021:S1096-7192(21)00819-2. [PMID: 34872807 DOI: 10.1016/j.ymgme.2021.11.001] [Reference Citation Analysis]
19 Morgan NV, Yngvadottir B, O'Driscoll M, Clark GR, Walsh D, Martin E, Tee L, Reid E, Titheradge HL, Maher ER. Evidence that autosomal recessive spastic cerebral palsy-1 (CPSQ1) is caused by a missense variant in HPDL. Brain Commun 2021;3:fcab002. [PMID: 33634263 DOI: 10.1093/braincomms/fcab002] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
20 Hakami WS, Hundallah KJ, Tabarki BM. Metabolic and genetic disorders mimicking cerebral palsy. Neurosciences (Riyadh) 2019;24:155-63. [PMID: 31380813 DOI: 10.17712/nsj.2019.3. 20190045] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Bonnefoy-Mazure A, De Coulon G, Lascombes P, Armand S. Follow-up of walking quality after end of growth in 28 children with bilateral cerebral palsy. J Child Orthop 2020;14:41-9. [PMID: 32165980 DOI: 10.1302/1863-2548.14.190125] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
22 Zech M, Jech R, Boesch S, Škorvánek M, Weber S, Wagner M, Zhao C, Jochim A, Necpál J, Dincer Y, Vill K, Distelmaier F, Stoklosa M, Krenn M, Grunwald S, Bock-Bierbaum T, Fečíková A, Havránková P, Roth J, Příhodová I, Adamovičová M, Ulmanová O, Bechyně K, Danhofer P, Veselý B, Haň V, Pavelekova P, Gdovinová Z, Mantel T, Meindl T, Sitzberger A, Schröder S, Blaschek A, Roser T, Bonfert MV, Haberlandt E, Plecko B, Leineweber B, Berweck S, Herberhold T, Langguth B, Švantnerová J, Minár M, Ramos-Rivera GA, Wojcik MH, Pajusalu S, Õunap K, Schatz UA, Pölsler L, Milenkovic I, Laccone F, Pilshofer V, Colombo R, Patzer S, Iuso A, Vera J, Troncoso M, Fang F, Prokisch H, Wilbert F, Eckenweiler M, Graf E, Westphal DS, Riedhammer KM, Brunet T, Alhaddad B, Berutti R, Strom TM, Hecht M, Baumann M, Wolf M, Telegrafi A, Person RE, Zamora FM, Henderson LB, Weise D, Musacchio T, Volkmann J, Szuto A, Becker J, Cremer K, Sycha T, Zimprich F, Kraus V, Makowski C, Gonzalez-Alegre P, Bardakjian TM, Ozelius LJ, Vetro A, Guerrini R, Maier E, Borggraefe I, Kuster A, Wortmann SB, Hackenberg A, Steinfeld R, Assmann B, Staufner C, Opladen T, Růžička E, Cohn RD, Dyment D, Chung WK, Engels H, Ceballos-Baumann A, Ploski R, Daumke O, Haslinger B, Mall V, Oexle K, Winkelmann J. Monogenic variants in dystonia: an exome-wide sequencing study. Lancet Neurol 2020;19:908-18. [PMID: 33098801 DOI: 10.1016/S1474-4422(20)30312-4] [Cited by in Crossref: 28] [Cited by in F6Publishing: 12] [Article Influence: 14.0] [Reference Citation Analysis]
23 Ebrahimi-Fakhari D, Teinert J, Behne R, Wimmer M, D'Amore A, Eberhardt K, Brechmann B, Ziegler M, Jensen DM, Nagabhyrava P, Geisel G, Carmody E, Shamshad U, Dies KA, Yuskaitis CJ, Salussolia CL, Ebrahimi-Fakhari D, Pearson TS, Saffari A, Ziegler A, Kölker S, Volkmann J, Wiesener A, Bearden DR, Lakhani S, Segal D, Udwadia-Hegde A, Martinuzzi A, Hirst J, Perlman S, Takiyama Y, Xiromerisiou G, Vill K, Walker WO, Shukla A, Dubey Gupta R, Dahl N, Aksoy A, Verhelst H, Delgado MR, Kremlikova Pourova R, Sadek AA, Elkhateeb NM, Blumkin L, Brea-Fernández AJ, Dacruz-Álvarez D, Smol T, Ghoumid J, Miguel D, Heine C, Schlump JU, Langen H, Baets J, Bulk S, Darvish H, Bakhtiari S, Kruer MC, Lim-Melia E, Aydinli N, Alanay Y, El-Rashidy O, Nampoothiri S, Patel C, Beetz C, Bauer P, Yoon G, Guillot M, Miller SP, Bourinaris T, Houlden H, Robelin L, Anheim M, Alamri AS, Mahmoud AAH, Inaloo S, Habibzadeh P, Faghihi MA, Jansen AC, Brock S, Roubertie A, Darras BT, Agrawal PB, Santorelli FM, Gleeson J, Zaki MS, Sheikh SI, Bennett JT, Sahin M. Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia. Brain 2020;143:2929-44. [PMID: 32979048 DOI: 10.1093/brain/awz307] [Cited by in Crossref: 2] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
24 Herzog R, Weissbach A, Bäumer T, Münchau A. Complex dystonias: an update on diagnosis and care. J Neural Transm (Vienna) 2021;128:431-45. [PMID: 33185802 DOI: 10.1007/s00702-020-02275-y] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
25 Deputy SR, Tilton AH. Treatment of Disorders of Tone and Other Considerations in Pediatric Movement Disorders. Neurotherapeutics 2020;17:1713-23. [PMID: 33410106 DOI: 10.1007/s13311-020-00984-6] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
26 Al Masseri Z, Alsayed M. Gonadal mosaicism in GNAO1 causing neurodevelopmental disorder with involuntary movements; two additional variants. Molecular Genetics and Metabolism Reports 2022;31:100864. [DOI: 10.1016/j.ymgmr.2022.100864] [Reference Citation Analysis]
27 Gilbert C, Sauer M, Cheng J. Reduction of self-mutilating behavior and improved oromotor function in a patient with Lesch-Nyhan syndrome following botulinum toxin injection: A case report. J Pediatr Rehabil Med 2021;14:133-6. [PMID: 33720862 DOI: 10.3233/PRM-200729] [Reference Citation Analysis]
28 Feraco P, Incandela F, Franceschi R, Gagliardo C, Bellizzi M. Clinical and Brain Imaging Findings in a Child with Vitamin B12 Deficiency. Pediatr Rep 2021;13:583-8. [PMID: 34842801 DOI: 10.3390/pediatric13040069] [Reference Citation Analysis]
29 Tang Y, Cao Z, Xia Y, Liu Y, Zhang W. Effectiveness and safety of pure acupuncture and moxibustion in the treatment of children with cerebral palsy: A protocol for systematic review and meta analysis. Medicine (Baltimore) 2021;100:e23907. [PMID: 33530188 DOI: 10.1097/MD.0000000000023907] [Reference Citation Analysis]
30 Aravamuthan BR, Shevell M, Kim YM, Wilson JL, O'Malley JA, Pearson TS, Kruer MC, Fahey M, Waugh JL, Russman B, Shapiro B, Tilton A. Role of child neurologists and neurodevelopmentalists in the diagnosis of cerebral palsy: A survey study. Neurology 2020;95:962-72. [PMID: 33046609 DOI: 10.1212/WNL.0000000000011036] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
31 Chin EM, Gwynn HE, Robinson S, Hoon AH Jr. Principles of Medical and Surgical Treatment of Cerebral Palsy. Neurol Clin 2020;38:397-416. [PMID: 32279717 DOI: 10.1016/j.ncl.2020.01.009] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]