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: 7052649)

  • 1. [Neonatal myoclonic encephalopathy. Contribution of a case with suspected dysmetabolic etiology].
    Vigevano F; Cincinnati P; Bertini E; Bosman C; Gisondi A; Maccagnani F
    Riv Neurobiol; 1981; 27(34):458-66. PubMed ID: 7052649
    [No Abstract]   [Full Text] [Related]  

  • 2. Infantile spasms (West syndrome) in children with inborn errors of metabolism: a review of the literature.
    Gkampeta A; Pavlou E
    J Child Neurol; 2012 Oct; 27(10):1295-301. PubMed ID: 22832779
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Brain damage in infants--brain lesions in several cases of inborn errors of metabolism].
    Kamoshita S
    Shinkei Kenkyu No Shimpo; 1972 Jun; 16(3):438-46. PubMed ID: 5066186
    [No Abstract]   [Full Text] [Related]  

  • 4. Postmortem findings in term neonates.
    Pinar H
    Semin Neonatol; 2004 Aug; 9(4):289-302. PubMed ID: 15251146
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The value of autopsy in determining the cause of failure to respond to resuscitation at birth.
    Squier W; Cowan FM
    Semin Neonatol; 2004 Aug; 9(4):331-45. PubMed ID: 15251149
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [2 families of a Valaisan isolate with infantile epileptogenic encephalopathy].
    Pescia G; Klein D; Wildi E
    Rev Otoneuroophtalmol; 1974; 46(5):483-9. PubMed ID: 4460174
    [No Abstract]   [Full Text] [Related]  

  • 7. Brain malformation and infantile spasms in a SCAD deficiency patient.
    Mikati MA; Chaaban HR; Karam PE; Krishnamoorthy KS
    Pediatr Neurol; 2007 Jan; 36(1):48-50. PubMed ID: 17162197
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Infantile myoclonic encephalopathy with hypsarrhythia associated with basilar artery aneurysm].
    Denes F; De Zanche L; Zanetti R
    Riv Sper Freniatr Med Leg Alien Ment; 1970 Apr; 94(2):377-85. PubMed ID: 5484961
    [No Abstract]   [Full Text] [Related]  

  • 9. [Diagnostic focus on the child with myoclonic seizures in isolation or associated with other types of seizures].
    Herranz JL; de las Cuevas I
    Rev Neurol; 1998 Feb; 26(150):301-7. PubMed ID: 9563099
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Epileptic encephalopathy and brain iron accumulation due to WDR45 mutation.
    Khoury J; Kotagal P; Moosa ANV
    Seizure; 2019 Oct; 71():245-246. PubMed ID: 31466010
    [No Abstract]   [Full Text] [Related]  

  • 11. [Disorder of histidine metabolism induced by anticonvulsant therapy during a familial myoclonic encephalopathy].
    Mozziconacci P; Boisse J; Attal C; Pham-Huu-Trung ; Lemonnier A; Lévy H
    Ann Pediatr (Paris); 1964 Mar; 11(3):176-87. PubMed ID: 5878706
    [No Abstract]   [Full Text] [Related]  

  • 12. Classification of infantile seizures: implications for identification and treatment of inborn errors of metabolism.
    Nordli DR; De Vivo DC
    J Child Neurol; 2002 Dec; 17 Suppl 3():3S3-7; discussion 3S8. PubMed ID: 12597050
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Therapeutic strategy in severe encephalopathies].
    Campos-Castelló J
    Rev Neurol; 2001 May 1-15; 32(9):860-6. PubMed ID: 11424039
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Perinatal cerebral lesions: topography, determining factors].
    Villegas H; Escobar A; Shor V; Karchmer S
    Ginecol Obstet Mex; 1975 Oct; 38(228):233-45. PubMed ID: 1205169
    [No Abstract]   [Full Text] [Related]  

  • 15. Brain development and the structural basis of perinatal brain damage.
    Wigglesworth JS
    Mead Johnson Symp Perinat Dev Med; 1980; (17):3-10. PubMed ID: 7345265
    [No Abstract]   [Full Text] [Related]  

  • 16. Cerebral capillary telangiectasis in an infant. Coincidental Association with hypsarrhythmia.
    Crosley CJ; Kim RC; Parisi JE; Collins GH; Sondheimer J
    Arch Pathol Lab Med; 1982 Feb; 106(2):79-80. PubMed ID: 6895831
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Central tegmental tract lesion in a girl with holoprosencephaly presenting with West syndrome.
    Yoshikawa H; Nakano K; Watanabe S
    Eur J Paediatr Neurol; 2009 Jul; 13(4):376-9. PubMed ID: 18692418
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Impairment of neocortical ontogenetic program leading to severe infantile encephalopathy with burst suppression.
    Spreafico R; Angelini L; Mastrangelo M; Rizzuti T; Bugiani O; Avanzini G
    Epilepsy Res Suppl; 1996; 12():79-87. PubMed ID: 9302506
    [No Abstract]   [Full Text] [Related]  

  • 19. Fatal congenital lactic acidosis in two siblings. I. Clinical and pathological findings.
    Lie SO; Löken AC; Strömme JH; Aagenaes O
    Acta Paediatr Scand; 1971 Mar; 60(2):129-37. PubMed ID: 5548117
    [No Abstract]   [Full Text] [Related]  

  • 20. [Inherited metabolic diseases associated with West syndrome].
    Wada K; Sakuragawa N
    Ryoikibetsu Shokogun Shirizu; 2002; (37 Pt 6):283-7. PubMed ID: 12483882
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.