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 *

127 related articles for article (PubMed ID: 32157690)

  • 21. Atypical motor behavior in a poststroke subject with agenesis of the corpus callosum: a case report.
    Pandian S; Arya KN
    Ann Phys Rehabil Med; 2014 Apr; 57(3):200-9. PubMed ID: 24680635
    [No Abstract]   [Full Text] [Related]  

  • 22. CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1.
    Fransen E; Lemmon V; Van Camp G; Vits L; Coucke P; Willems PJ
    Eur J Hum Genet; 1995; 3(5):273-84. PubMed ID: 8556302
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Agenesis of the corpus callosum].
    Maksić J; Raicević R; Obradović D; Rajsić N; Popović S; Vladejić S
    Vojnosanit Pregl; 2003; 60(2):233-6. PubMed ID: 12852169
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Agenesis of the corpus callosum: neonatal sonographic detection.
    Penny SM
    Radiol Technol; 2006; 78(1):14-8. PubMed ID: 16998191
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Congenital mirror movements: no mutation in DNAL4 in 17 index cases.
    Méneret A; Trouillard O; Vidailhet M; Depienne C; Roze E
    J Neurol; 2014 Oct; 261(10):2030-1. PubMed ID: 25236653
    [No Abstract]   [Full Text] [Related]  

  • 26. Congenital Mirror Movements Due to RAD51: Cosegregation with a Nonsense Mutation in a Norwegian Pedigree and Review of the Literature.
    Trouillard O; Koht J; Gerstner T; Moland S; Depienne C; Dusart I; Méneret A; Ruiz M; Dubacq C; Roze E
    Tremor Other Hyperkinet Mov (N Y); 2016; 6():424. PubMed ID: 27830107
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Novel ABCD1 Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum.
    Qiu Y; Xin L; Wang Y; Yu Y; Zou K; Zhou Q; Chen Y; Chen S; Zhu M; Hong D
    Neurodegener Dis; 2018; 18(2-3):156-164. PubMed ID: 29966135
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A mother and daughter with agenesis of the corpus callosum.
    Fuchigami T; Mazaki R; Nishimura A; Noguchi Y; Fuchigami S; Fujita Y; Okubo O; Harada K
    Acta Paediatr Jpn; 1996 Feb; 38(1):52-6. PubMed ID: 8992860
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Heterozygous variants in
    Thams S; Islam M; Lindefeldt M; Nordgren A; Granberg T; Tesi B; Barbany G; Nilsson D; Paucar M
    Neurol Genet; 2020 Dec; 6(6):e526. PubMed ID: 33209984
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Lateralization of motor control in the human nervous system: genetics of mirror movements.
    Peng J; Charron F
    Curr Opin Neurobiol; 2013 Feb; 23(1):109-18. PubMed ID: 22989473
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Corpus callosum agenesis.
    Chacko A; Koul R; Sankhla DK
    Saudi Med J; 2001 Jan; 22(1):22-5. PubMed ID: 11255605
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Agenesis of the corpus callosum. 1. Neuropsychological studies.
    Ferriss GS; Dorsen MM
    Cortex; 1975 Jun; 11(2):95-122. PubMed ID: 1149479
    [No Abstract]   [Full Text] [Related]  

  • 33. Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midline.
    Welniarz Q; Morel MP; Pourchet O; Gallea C; Lamy JC; Cincotta M; Doulazmi M; Belle M; Méneret A; Trouillard O; Ruiz M; Brochard V; Meunier S; Trembleau A; Vidailhet M; Chédotal A; Dusart I; Roze E
    Sci Rep; 2017 Mar; 7(1):410. PubMed ID: 28341853
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Interhemispheric lipoma associated with agenesis of the corpus callosum.
    Jiménez Caballero PE
    Neurologia; 2012 Oct; 27(8):515-7. PubMed ID: 21890243
    [No Abstract]   [Full Text] [Related]  

  • 35. MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosum.
    Bader I; Decker E; Mayr JA; Lunzer V; Koch J; Boltshauser E; Sperl W; Pietsch P; Ertl-Wagner B; Bolz H; Bergmann C; Rittinger O
    Eur J Med Genet; 2016 Aug; 59(8):386-91. PubMed ID: 27377014
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel DCC mutation and genetic heterogeneity in congenital mirror movements.
    Depienne C; Cincotta M; Billot S; Bouteiller D; Groppa S; Brochard V; Flamand C; Hubsch C; Meunier S; Giovannelli F; Klebe S; Corvol JC; Vidailhet M; Brice A; Roze E
    Neurology; 2011 Jan; 76(3):260-4. PubMed ID: 21242494
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation.
    Demirayak P; Onat OE; Gevrekci AÖ; Gülsüner S; Uysal H; Bilgen RS; Doerschner K; Özçelik TS; Boyacı H
    Diagn Interv Radiol; 2018 Nov; 24(6):392-401. PubMed ID: 30406765
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Agenesis of the corpus callosum in Schinzel-Giedion syndrome associated with 47,XXY karyotype.
    Ozkinay FF; Akisü M; Kültürsay N; Oral R; Tansug N; Sapmaz G
    Clin Genet; 1996 Sep; 50(3):145-8. PubMed ID: 8946113
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Congenital cranial dysinnervation disorder in a boy with congenital mirror movements.
    Al Shamrani M; Mahmoudi F; Abu-Amero KK; Khan AO
    J AAPOS; 2015 Apr; 19(2):191-2. PubMed ID: 25838174
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Agenesis of the Corpus Callosum and Generalized Epilepsy.
    Ilik F; Bilgilisoy UT
    Clin EEG Neurosci; 2015 Jul; 46(3):253-5. PubMed ID: 24997010
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.