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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

189 related items for PubMed ID: 21238681

  • 1. Unusual coexistence of caudal duplication and caudal regression syndromes.
    Bansal G, Ghosh D, George U, Bhatti W.
    J Pediatr Surg; 2011 Jan; 46(1):256-8. PubMed ID: 21238681
    [Abstract] [Full Text] [Related]

  • 2. [Caudal regression syndrome].
    Khemakhem R, Toumia HB, Francoise Ben Dridi M, Chaouachi B.
    Tunis Med; 2012 Apr; 90(4):342. PubMed ID: 22535352
    [No Abstract] [Full Text] [Related]

  • 3. Currarino syndrome: typical images of a rare condition.
    Leonard D, Pendlimari R, Larson DW, Dozois EJ.
    Tech Coloproctol; 2010 Sep; 14(3):289-90. PubMed ID: 20502931
    [No Abstract] [Full Text] [Related]

  • 4. Juvenile glaucoma in a child with caudal regression syndrome.
    Moberg J, Uchaeva L, Holm C, Koranyi G.
    Acta Ophthalmol; 2011 Sep; 89(6):e534-5. PubMed ID: 20809909
    [No Abstract] [Full Text] [Related]

  • 5. [Congenital anomalies in the central nervous system (6) occult spinal dysraphism (other than spinal lipoma): congenital dermal sinus, tight filum terminale, neurenteric cyst, split cord malformation, and caudal regression syndrome].
    Shigeta H.
    No Shinkei Geka; 2011 May; 39(5):513-27. PubMed ID: 21512203
    [No Abstract] [Full Text] [Related]

  • 6. Teaching NeuroImages: caudal regression syndrome.
    Sharma S, Jana M.
    Neurology; 2011 Dec 13; 77(24):e149. PubMed ID: 22170950
    [No Abstract] [Full Text] [Related]

  • 7. Mutation analysis of the motor neuron and pancreas homeobox 1 (MNX1, former HLXB9) gene in Swedish patients with Currarino syndrome.
    Zu S, Winberg J, Arnberg F, Palmer G, Svensson PJ, Wester T, Nordenskjöld A.
    J Pediatr Surg; 2011 Jul 13; 46(7):1390-5. PubMed ID: 21763840
    [Abstract] [Full Text] [Related]

  • 8. Caudal regression syndrome with bilateral popliteal webbing without maternal diabetes: a rare entity.
    Aggarwal M, Sood V, Deswal S, Aggarwal KC.
    Childs Nerv Syst; 2012 Oct 13; 28(10):1819-21. PubMed ID: 22526445
    [No Abstract] [Full Text] [Related]

  • 9. [Caudal regression syndrome - caudal agenesis].
    van Baalen A, Jacobs J, Alfke K, Caliebe A, Stephani U.
    Klin Padiatr; 2008 Oct 13; 220(2):86-7. PubMed ID: 18098097
    [Abstract] [Full Text] [Related]

  • 10. A Rare Cause of Chronic Constipation.
    Phipps KD, Wrogemann J, El-Matary W.
    Gastroenterology; 2016 May 13; 150(5):1090-1091. PubMed ID: 27020335
    [No Abstract] [Full Text] [Related]

  • 11. Presentation of incomplete Currarino triad in a 12-day-old patient with vomiting: a case report.
    Kasem AJ, Pottker T.
    Pediatr Emerg Care; 2013 Jul 13; 29(7):836-7. PubMed ID: 23823266
    [Abstract] [Full Text] [Related]

  • 12. Syringomyelia in caudal dysplasia sequence.
    Basu S, Nair N.
    J Assoc Physicians India; 2003 Aug 13; 51():820-3. PubMed ID: 14651150
    [Abstract] [Full Text] [Related]

  • 13. Currarino syndrome: variable imaging features in three siblings with HLXB9 gene mutation.
    Kim AY, Yoo SY, Kim JH, Eo H, Jeon TY.
    Clin Imaging; 2013 Aug 13; 37(2):398-402. PubMed ID: 23466002
    [Abstract] [Full Text] [Related]

  • 14. Neonatal Currarino's syndrome presenting as intestinal obstruction.
    Patel RV, Shepherd G, Kumar H, Patwardhan N.
    BMJ Case Rep; 2013 Oct 15; 2013():. PubMed ID: 24130205
    [No Abstract] [Full Text] [Related]

  • 15. Currarinot triade.
    Boettcher M, Krebs TF.
    ANZ J Surg; 2012 Apr 15; 82(4):275. PubMed ID: 22510187
    [No Abstract] [Full Text] [Related]

  • 16. Caudal regression syndrome in one of dizygotic twins.
    Krenova Z, Elstnerova L, Dolezel Z, Kren L.
    Fetal Pediatr Pathol; 2010 Apr 15; 29(6):419-23. PubMed ID: 21043567
    [Abstract] [Full Text] [Related]

  • 17. Familial Currarino syndrome associated with Hirschsprung disease: two cases of a mother and daughter.
    Ohno K, Nakamura T, Azuma T, Nakaoka T, Takama Y, Hayashi H, Horiike M, Zenitani M, Higashio A.
    J Pediatr Surg; 2013 Jan 15; 48(1):233-8. PubMed ID: 23331821
    [Abstract] [Full Text] [Related]

  • 18. [Currarino syndrome].
    Estévez M, Miner I, Benito MA, Calvo C, Corcuera P, Nogués A, Eizaguirre I.
    Cir Pediatr; 2008 Jan 15; 21(1):49-51. PubMed ID: 18444392
    [Abstract] [Full Text] [Related]

  • 19. Caudal regression syndrome associated with the white matter lesions and chromosome 18p11.2 deletion.
    Kaciński M, Jaworek M, Skowronek-Bała B.
    Brain Dev; 2007 Apr 15; 29(3):164-6. PubMed ID: 16949239
    [Abstract] [Full Text] [Related]

  • 20. [Image of the month. Abnormal gluteal crease revealing Currarino syndrome].
    Jedidi Z, Moonen G.
    Rev Med Liege; 2012 Oct 15; 67(10):499-500. PubMed ID: 23167156
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.