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 *

59 related articles for article (PubMed ID: 13109176)

  • 21. Ataxia-telangiectasia in Iran: clinical and laboratory features of 104 patients.
    Moin M; Aghamohammadi A; Kouhi A; Tavassoli S; Rezaei N; Ghaffari SR; Gharagozlou M; Movahedi M; Purpak Z; Mirsaeid Ghazi B; Mahmoudi M; Farhoudi A
    Pediatr Neurol; 2007 Jul; 37(1):21-8. PubMed ID: 17628218
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Alpha-lipoic acid reduces congenital malformations in the offspring of diabetic mice.
    Sugimura Y; Murase T; Kobayashi K; Oyama K; Hayasaka S; Kanou Y; Oiso Y; Murata Y
    Diabetes Metab Res Rev; 2009 Mar; 25(3):287-94. PubMed ID: 19242917
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Progressive ataxia and palatal tremor (PAPT): clinical and MRI assessment with review of palatal tremors.
    Samuel M; Torun N; Tuite PJ; Sharpe JA; Lang AE
    Brain; 2004 Jun; 127(Pt 6):1252-68. PubMed ID: 15090471
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Isoametropic amblyopia in highly hyperopic children.
    Ziylan S; Yabas O; Zorlutuna N; Serin D
    Acta Ophthalmol Scand; 2007 Feb; 85(1):111-3. PubMed ID: 17244222
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Some familial congenital malformations.
    Williamson EM
    Midwives Chron; 1966 Oct; 79(945):388-9. PubMed ID: 5179695
    [No Abstract]   [Full Text] [Related]  

  • 26. [A new syndrome of multiple malformations: skeletal malformations of the spinal column, hands and ectopic solitary kidney].
    GROSSI-BIANCHI ML; BRUNI R
    Minerva Pediatr; 1958 Dec; 10(49):1457-63. PubMed ID: 13643931
    [No Abstract]   [Full Text] [Related]  

  • 27. [One year prevalence of mental disorders comorbidity and associated socio-demographic risk factors in the general population of Spain. Results of the ESEMeD-Spain study].
    Autonell J; Vila F; Pinto-Meza A; Vilagut G; Codony M; Almansa J; Muñoz PE; Torres JV; Alonso J; Haro JM
    Actas Esp Psiquiatr; 2007 Sep; 35 Suppl 2():4-11. PubMed ID: 18264864
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Risk of major congenital malformations associated with infertility and its treatment by extent of iatrogenic intervention.
    Farhi J; Fisch B
    Pediatr Endocrinol Rev; 2007 Jun; 4(4):352-7. PubMed ID: 17643083
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Ocular flutter, generalized myoclonus, and trunk ataxia associated with anti-GQ1b antibodies.
    Zaro-Weber O; Galldiks N; Dohmen C; Fink GR; Nowak DA
    Arch Neurol; 2008 May; 65(5):659-61. PubMed ID: 18474744
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Congenital malformations and induction disorders].
    ROSSELLI D
    Minerva Chir; 1958 Sep; 13(17):948-58. PubMed ID: 13600074
    [No Abstract]   [Full Text] [Related]  

  • 31. [Gillespie syndrome: 2 familial cases].
    Boughamoura L; Yacoub M; Abroug M; Chabchoub I; Bouguezzi R; Charfeddine L; Amri F; Essoussi AS
    Arch Pediatr; 2006 Oct; 13(10):1323-5. PubMed ID: 16919425
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The adult form of Niemann-Pick disease type C.
    Sévin M; Lesca G; Baumann N; Millat G; Lyon-Caen O; Vanier MT; Sedel F
    Brain; 2007 Jan; 130(Pt 1):120-33. PubMed ID: 17003072
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Vestibular, saccadic and fixation abnormalities in genetically confirmed Friedreich ataxia.
    Fahey MC; Cremer PD; Aw ST; Millist L; Todd MJ; White OB; Halmagyi M; Corben LA; Collins V; Churchyard AJ; Tan K; Kowal L; Delatycki MB
    Brain; 2008 Apr; 131(Pt 4):1035-45. PubMed ID: 18238798
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Non-movement disorder heralds symptoms of Machado-Joseph disease years before ataxia.
    D'Abreu A; Friedman J; Coskun J
    Mov Disord; 2005 Jun; 20(6):739-41. PubMed ID: 15747372
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Spectrum of pediatric developmental and genetic renal lesions and associated congenital malformations--an autopsy study from north India.
    Kakkar N; Menon S; Radotra BD
    Fetal Pediatr Pathol; 2006; 25(1):35-49. PubMed ID: 16754487
    [TBL] [Abstract][Full Text] [Related]  

  • 36. FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy.
    Biancalana V; Toft M; Le Ber I; Tison F; Scherrer E; Thibodeau S; Mandel JL; Brice A; Farrer MJ; Dürr A
    Arch Neurol; 2005 Jun; 62(6):962-6. PubMed ID: 15956167
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Profile of major congenital malformations in neonates in Al-Jahra region of Kuwait.
    Madi SA; Al-Naggar RL; Al-Awadi SA; Bastaki LA
    East Mediterr Health J; 2005 Jul; 11(4):700-6. PubMed ID: 16700386
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Ocular malformations as dysraphic manifestations].
    DONI A
    Riv Neurol; 1954; 24(2):236-42. PubMed ID: 13195496
    [No Abstract]   [Full Text] [Related]  

  • 39. Clinical evaluation of cessation of hyperopia in 123 children with accommodative esotropia treated with glasses for best corrected vision.
    Cho YA; Yi S; Kim SW
    Acta Ophthalmol; 2009 Aug; 87(5):532-7. PubMed ID: 18759801
    [TBL] [Abstract][Full Text] [Related]  

  • 40. SYNDROMES OF KLIPPEL-TR'ENAUNAY AND STURGE-WEBER IN THE SAME PATIENT.
    KRAMER W
    Psychiatr Neurol Neurochir; 1963; 66():362-70. PubMed ID: 14062200
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 3.