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 *

168 related articles for article (PubMed ID: 23072181)

  • 1. Pontocerebellar hypoplasia associated with nevoid hyperpigmentation and dysmorphic findings: a new subtype?
    Sonmez FM; Yayli S; Kul S; Celep F; Ozkaya AK; Ersoz S; Erpolat S
    Genet Couns; 2012; 23(3):347-52. PubMed ID: 23072181
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pontocerebellar hypoplasia type 3 with severe vitamin A deficiency.
    Jacob FD; Hasal S; Goez HR
    Pediatr Neurol; 2011 Feb; 44(2):147-9. PubMed ID: 21215917
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recurrent episodes of rhabdomyolysis in pontocerebellar hypoplasia type 2.
    Zafeiriou DI; Ververi A; Tsitlakidou A; Anastasiou A; Vargiami E
    Neuromuscul Disord; 2013 Feb; 23(2):116-9. PubMed ID: 23177318
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The very low density lipoprotein receptor-associated pontocerebellar hypoplasia and dysmorphic features in three Turkish patients.
    Sonmez FM; Gleeson JG; Celep F; Kul S
    J Child Neurol; 2013 Mar; 28(3):379-83. PubMed ID: 22532556
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pontocerebellar hypoplasia: review of classification and genetics, and exclusion of several genes known to be important for cerebellar development.
    Maricich SM; Aqeeb KA; Moayedi Y; Mathes EL; Patel MS; Chitayat D; Lyon G; Leroy JG; Zoghbi HY
    J Child Neurol; 2011 Mar; 26(3):288-94. PubMed ID: 21383226
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Pontocerebellar hypoplasia type 1: a case report].
    Gómez-Lado C; Landín-Iglesias G; Pintos-Martínez E; Pastor-Benavent N; Eirís-Puñal J; Castro-Gago M
    Rev Neurol; 2007 Mar 1-15; 44(5):281-4. PubMed ID: 17342678
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pontocerebellar hypoplasia type 3 with tetralogy of Fallot.
    Jinnou H; Okanishi T; Enoki H; Ohki S
    Brain Dev; 2012 May; 34(5):392-5. PubMed ID: 21880448
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Autopsy case of later-onset pontocerebellar hypoplasia type 1: pontine atrophy and pyramidal tract involvement.
    Sanefuji M; Kira R; Matsumoto K; Gondo K; Torisu H; Kawakami H; Iwaki T; Hara T
    J Child Neurol; 2010 Nov; 25(11):1429-34. PubMed ID: 20558670
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Delayed gyration with pontocerebellar hypoplasia type 1.
    Okanishi T; Mori Y; Shirai K; Kobayashi S; Nakashima H; Kibe T; Yokochi K; Togari H; Nonaka I
    Brain Dev; 2010 Mar; 32(3):258-62. PubMed ID: 19243903
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pontocerebellar hypoplasia in two siblings with dysmorphic features.
    Dilber E; Aynaci FM; Ahmetoglu A
    J Child Neurol; 2002 Jan; 17(1):64-6. PubMed ID: 11913577
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial pontocerebellar hypoplasia type I with anterior horn cell disease.
    Görgen-Pauly U; Sperner J; Reiss I; Gehl HB; Reusche E
    Eur J Paediatr Neurol; 1999; 3(1):33-8. PubMed ID: 10727190
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pontocerebellar hypoplasia type 2: a neuropathological update.
    Barth PG; Aronica E; de Vries L; Nikkels PG; Scheper W; Hoozemans JJ; Poll-The BT; Troost D
    Acta Neuropathol; 2007 Oct; 114(4):373-86. PubMed ID: 17641900
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pontocerebellar hypoplasia associated with respiratory-chain defects.
    de Koning TJ; de Vries LS; Groenendaal F; Ruitenbeek W; Jansen GH; Poll-The BT; Barth PG
    Neuropediatrics; 1999 Apr; 30(2):93-5. PubMed ID: 10401692
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lethal olivopontoneocerebellar hypoplasia with dysmorphic features in sibs.
    Young ID; McKeever PA; Squier MV; Grant J
    J Med Genet; 1992 Oct; 29(10):733-5. PubMed ID: 1433235
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis.
    Hartmann A; Hofmann UB; Hoehn H; Broecker EB; Hamm H
    Pediatr Dermatol; 2004; 21(6):636-41. PubMed ID: 15575846
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Progress on pontocerebellar hypoplasia.
    Hevner RF
    Acta Neuropathol; 2007 Oct; 114(4):401-2. PubMed ID: 17710422
    [No Abstract]   [Full Text] [Related]  

  • 17. Pontocerebellar hypoplasia in extreme prematurity: clinical and neuroimaging findings.
    Zafeiriou DI; Ververi A; Anastasiou A; Soubasi V; Vargiami E
    Pediatr Neurol; 2013 Jan; 48(1):48-51. PubMed ID: 23290020
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Linear and whorled hypermelanosis.
    Di Lernia V
    Pediatr Dermatol; 2007; 24(3):205-10. PubMed ID: 17542865
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Linear and whorled nevoid hypermelanosis.
    Yuksek J; Sezer E; Erbil AH; Arca E; Taştan HB; Kurumlu Z; Demiriz M
    Dermatol Online J; 2007 Jul; 13(3):23. PubMed ID: 18328217
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Extended phenotype of pontocerebellar hypoplasia with infantile spinal muscular atrophy.
    Rudnik-Schöneborn S; Sztriha L; Aithala GR; Houge G; Laegreid LM; Seeger J; Huppke M; Wirth B; Zerres K
    Am J Med Genet A; 2003 Feb; 117A(1):10-7. PubMed ID: 12548734
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.