These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 37757660)

  • 41. Novel Homozygous Variant in TTC19 Causing Mitochondrial Complex III Deficiency with Recurrent Stroke-Like Episodes: Expanding the Phenotype.
    Conboy E; Selcen D; Brodsky M; Gavrilova R; Ho ML
    Semin Pediatr Neurol; 2018 Jul; 26():16-20. PubMed ID: 29961508
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Disruption of basal lamina components in neuromotor synapses of children with spastic quadriplegic cerebral palsy.
    Robinson KG; Mendonca JL; Militar JL; Theroux MC; Dabney KW; Shah SA; Miller F; Akins RE
    PLoS One; 2013; 8(8):e70288. PubMed ID: 23976945
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Whole exome sequencing of suspected mitochondrial patients in clinical practice.
    Wortmann SB; Koolen DA; Smeitink JA; van den Heuvel L; Rodenburg RJ
    J Inherit Metab Dis; 2015 May; 38(3):437-43. PubMed ID: 25735936
    [TBL] [Abstract][Full Text] [Related]  

  • 44. New generation genetic testing entering the clinic.
    Gorcenco S; Ilinca A; Almasoudi W; Kafantari E; Lindgren AG; Puschmann A
    Parkinsonism Relat Disord; 2020 Apr; 73():72-84. PubMed ID: 32273229
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Clinical Application of Targeted Next-Generation Sequencing Panels and Whole Exome Sequencing in Childhood Epilepsy.
    Costain G; Cordeiro D; Matviychuk D; Mercimek-Andrews S
    Neuroscience; 2019 Oct; 418():291-310. PubMed ID: 31487502
    [TBL] [Abstract][Full Text] [Related]  

  • 46. ASXL3 De Novo Variant-Related Neurodevelopmental Disorder Presenting as Dystonic Cerebral Palsy.
    Švantnerová J; Minár M; Radová S; Kolníková M; Vlkovič P; Zech M
    Neuropediatrics; 2022 Oct; 53(5):361-365. PubMed ID: 35863334
    [No Abstract]   [Full Text] [Related]  

  • 47. Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia.
    Méreaux JL; Banneau G; Papin M; Coarelli G; Valter R; Raymond L; Kol B; Ariste O; Parodi L; Tissier L; Mairey M; Ait Said S; Gautier C; Guillaud-Bataille M; ; Forlani S; de la Grange P; Brice A; Vazza G; Durr A; Leguern E; Stevanin G
    Brain; 2022 Apr; 145(3):1029-1037. PubMed ID: 34983064
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Children with dyskinetic cerebral palsy are severely affected as compared to bilateral spastic cerebral palsy.
    Préel M; Rackauskaite G; Larsen ML; Laursen B; Lorentzen J; Born AP; Langhoff-Roos J; Uldall P; Hoei-Hansen CE
    Acta Paediatr; 2019 Oct; 108(10):1850-1856. PubMed ID: 30933377
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [A clinical study of cerebral palsy in Shiga; 1977-1986--III. Diagnosis and treatment of various types of cerebral palsy].
    Suzuki J; Ito M; Tomiwa K; Okuno T
    No To Hattatsu; 1999 Jul; 31(4):343-7. PubMed ID: 10429484
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Targeted exome sequencing for mitochondrial disorders reveals high genetic heterogeneity.
    DaRe JT; Vasta V; Penn J; Tran NT; Hahn SH
    BMC Med Genet; 2013 Nov; 14():118. PubMed ID: 24215330
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Etiologic yield of cerebral palsy: a contemporary case series.
    Shevell MI; Majnemer A; Morin I
    Pediatr Neurol; 2003 May; 28(5):352-9. PubMed ID: 12878296
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Children with congenital spastic hemiplegia obey Fitts' Law in a visually guided tapping task.
    Smits-Engelsman BC; Rameckers EA; Duysens J
    Exp Brain Res; 2007 Mar; 177(4):431-9. PubMed ID: 17019607
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Clinical and neuroimaging phenotypes of genetic parkinsonism from infancy to adolescence.
    Morales-Briceño H; Mohammad SS; Post B; Fois AF; Dale RC; Tchan M; Fung VSC
    Brain; 2020 Mar; 143(3):751-770. PubMed ID: 31800013
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A child with a novel DDX3X variant mimicking cerebral palsy: a case report.
    Hu L; Xin X; Lin S; Luo M; Chen J; Qiu H; Ma L; Huang J
    Ital J Pediatr; 2020 Jun; 46(1):88. PubMed ID: 32600431
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Dyskinetic strabismus as a sign of cerebral palsy.
    Buckley E; Seaber JH
    Am J Ophthalmol; 1981 May; 91(5):652-7. PubMed ID: 7234949
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Altered gene expression levels of genes related to muscle function in adults with cerebral palsy.
    Pingel J; Vandenrijt J; Kampmann ML; Andersen JD
    Tissue Cell; 2022 Jun; 76():101744. PubMed ID: 35151178
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Phenotype-driven variant filtration strategy in exome sequencing toward a high diagnostic yield and identification of 85 novel variants in 400 patients with rare Mendelian disorders.
    Marinakis NM; Svingou M; Veltra D; Kekou K; Sofocleous C; Tilemis FN; Kosma K; Tsoutsou E; Fryssira H; Traeger-Synodinos J
    Am J Med Genet A; 2021 Aug; 185(8):2561-2571. PubMed ID: 34008892
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Paroxysmal Movement Disorders: Recent Advances.
    Xu Z; Lim CK; Tan LCS; Tan EK
    Curr Neurol Neurosci Rep; 2019 Jun; 19(7):48. PubMed ID: 31187296
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Identification of pathways and genes associated with cerebral palsy.
    Zhu Q; Ni Y; Wang J; Yin H; Zhang Q; Zhang L; Bian W; Liang B; Kong L; Xuan L; Lu N
    Genes Genomics; 2018 Dec; 40(12):1339-1349. PubMed ID: 30109564
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Genetic counseling considerations in cerebral palsy.
    Elliott AM; Guimond C
    Mol Genet Metab; 2022 Dec; 137(4):428-435. PubMed ID: 34389249
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.