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Journal Abstract Search

161 related items for PubMed ID: 14872375

  • 1. [Osseous abnormalities and CT findings in Stueve-Wiedemann-Syndrome (SWS)].
    Langer R, Al-Gazali L, Haas D, Raupp P, Varady E.
    Rofo; 2004 Feb; 176(2):215-21. PubMed ID: 14872375
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  • 3. Presentation of six cases of Stüve-Wiedemann syndrome.
    Cormier-Daire V, Munnich A, Lyonnet S, Rustin P, Delezoide AL, Maroteaux P, Le Merrer M.
    Pediatr Radiol; 1998 Oct; 28(10):776-80. PubMed ID: 9799300
    [Abstract] [Full Text] [Related]

  • 4. Clinical homogeneity of the Stüve-Wiedemann syndrome and overlap with the Schwartz-Jampel syndrome type 2.
    Cormier-Daire V, Superti-Furga A, Munnich A, Lyonnet S, Rustin P, Delezoide AL, De Lonlay P, Giedion A, Maroteaux P, Le Merrer M.
    Am J Med Genet; 1998 Jun 30; 78(2):146-9. PubMed ID: 9674905
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  • 5. Stüve-Wiedemann syndrome and defects of the mitochondrial respiratory chain.
    Chabrol B, Sigaudy S, Paquis V, Montfort MF, Giudicelli H, Pellissier JF, Millet V, Mancini J, Philip N.
    Am J Med Genet; 1997 Oct 17; 72(2):222-6. PubMed ID: 9382147
    [Abstract] [Full Text] [Related]

  • 6. Cardiovascular abnormalities associated with the Stuve-Wiedemann syndrome.
    Raas-Rothschild A, Ergaz-Schaltiel Z, Bar-Ziv J, Rein AJ.
    Am J Med Genet A; 2003 Aug 30; 121A(2):156-8. PubMed ID: 12910496
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  • 7. Abnormal oral-pharyngeal swallowing as cause of morbidity and early death in Stüve-Wiedemann syndrome.
    Corona-Rivera JR, Cormier-Daire V, Dagoneau N, Coello-Ramírez P, López-Marure E, Romo-Huerta CO, Silva-Baez H, Aguirre-Salas LM, Estrada-Solorio MI.
    Eur J Med Genet; 2009 Aug 30; 52(4):242-6. PubMed ID: 19371797
    [Abstract] [Full Text] [Related]

  • 8. Schwartz-Jampel syndrome type 2 and Stüve-Wiedemann syndrome: a case for "lumping".
    Superti-Furga A, Tenconi R, Clementi M, Eich G, Steinmann B, Boltshauser E, Giedion A.
    Am J Med Genet; 1998 Jun 30; 78(2):150-4. PubMed ID: 9674906
    [Abstract] [Full Text] [Related]

  • 9. Stüve-Wiedemann syndrome in children surviving infancy: clinical and radiological features.
    Al-Gazali LI, Ravenscroft A, Feng A, Shubbar A, Al-Saggaf A, Haas D.
    Clin Dysmorphol; 2003 Jan 30; 12(1):1-8. PubMed ID: 12514358
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  • 11. Stuve-Wiedemann syndrome: a skeletal dysplasia characterized by bowed long bones.
    Begam MA, Alsafi W, Bekdache GN, Chedid F, Al-Gazali L, Mirghani HM.
    Ultrasound Obstet Gynecol; 2011 Nov 30; 38(5):553-8. PubMed ID: 21337444
    [Abstract] [Full Text] [Related]

  • 12. [Stüve-Wiedemann syndrome in two siblings: focusing on a male patient with the longest actual survival rate].
    Reither M, Urban M, Kozlowski KS, Pritsch M, Tegtmeyer FK.
    Klin Padiatr; 2006 Nov 30; 218(2):79-84. PubMed ID: 16506108
    [Abstract] [Full Text] [Related]

  • 13. Bronchopulmonary dysplasia: value of CT in identifying pulmonary sequelae.
    Oppenheim C, Mamou-Mani T, Sayegh N, de Blic J, Scheinmann P, Lallemand D.
    AJR Am J Roentgenol; 1994 Jul 30; 163(1):169-72. PubMed ID: 8010206
    [Abstract] [Full Text] [Related]

  • 14. The facio-digito-genital syndrome (Aarskog syndrome): a further delineation of the distinct radiological findings.
    Lizcano-Gil LA, Garcia-Cruz D, Cantu JM, Fryns JP.
    Genet Couns; 1994 Jul 30; 5(4):387-92. PubMed ID: 7888143
    [Abstract] [Full Text] [Related]

  • 15. Central nervous system malformations, dense bones and facial dysmorphism: a new autosomal recessive syndrome.
    al-Gazali LI, Bakalinova D, Bakir M.
    Clin Dysmorphol; 1998 Apr 30; 7(2):123-6. PubMed ID: 9571283
    [Abstract] [Full Text] [Related]

  • 16. Stuve Wiedemann syndrome and related syndromes: case report and possible anesthetic complications.
    Bonthuis D, Morava E, Booij LH, Driessen JJ.
    Paediatr Anaesth; 2009 Mar 30; 19(3):212-7. PubMed ID: 19207241
    [Abstract] [Full Text] [Related]

  • 17. Delineation of the clinical and radiological features of Stuve-Wiedemann syndrome childhood survivors, four new cases and review of the literature.
    Siccha SM, Cueto AM, Parrón-Pajares M, González-Morán G, Pacio-Miguez M, Del Pozo Á, Solís M, Rodriguez-Jimenez C, Caino S, Fano V, Heath KE, García-Miñaúr S, Palomares-Bralo M, Santos-Simarro F.
    Am J Med Genet A; 2021 Mar 30; 185(3):856-865. PubMed ID: 33305909
    [Abstract] [Full Text] [Related]

  • 18. A case of acampomelic campomelic dysplasia.
    Ozkilic A, Seven M, Yuksel A.
    Genet Couns; 2002 Mar 30; 13(1):23-8. PubMed ID: 12017234
    [Abstract] [Full Text] [Related]

  • 19. Asphyxiating thoracic dystrophy of the newborn.
    Sharma S.
    P N G Med J; 1983 Mar 30; 26(3-4):235-8. PubMed ID: 6595894
    [Abstract] [Full Text] [Related]

  • 20. Radiographic findings in Shprintzen-Goldberg syndrome.
    Nishimura G, Nagai T.
    Pediatr Radiol; 1996 Nov 30; 26(11):775-8. PubMed ID: 8929375
    [Abstract] [Full Text] [Related]

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