BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 24477277)

  • 1. Long-term follow-up in Stuve-Wiedemann syndrome: a case report with articular involvement.
    Buonuomo PS; Macchiaiolo M; Cambiaso P; Rana I; Digilio MC; Bartuli A
    Clin Dysmorphol; 2014 Apr; 23(2):45-46. PubMed ID: 24477277
    [No Abstract]   [Full Text] [Related]  

  • 2. Stüve-Wiedemann syndrome in a neonate.
    Sarafidis K; Piretzi K; Agakidou E; Kohlhase J; Zafeiriou D
    Pediatr Int; 2015 Apr; 57(2):302-4. PubMed ID: 25868946
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Stüve-Wiedemann syndrome: recurrent neonatal infections caused by impairment of JAK/STAT 3 pathway.
    Van De Maele K; Smulders C; Ecury-Goossen G; Rosina-Angelista I; Redeker E; van Haelst M
    Clin Dysmorphol; 2019 Apr; 28(2):57-62. PubMed ID: 30614825
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Stuve-Wiedemann syndrome: is it underrecognized?
    Yeşil G; Lebre AS; Santos SD; Güran O; Özahi II; Daire VC; Güran T
    Am J Med Genet A; 2014 Sep; 164A(9):2200-5. PubMed ID: 24988918
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Stüve-Wiedemann syndrome: LIFR and associated cytokines in clinical course and etiology.
    Mikelonis D; Jorcyk CL; Tawara K; Oxford JT
    Orphanet J Rare Dis; 2014 Mar; 9():34. PubMed ID: 24618404
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Stuve-Wiedemann syndrome with a novel mutation.
    Knipe M; Stanbury R; Unger S; Chakraborty M
    BMJ Case Rep; 2015 Aug; 2015():. PubMed ID: 26323980
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Stüve-Wiedemann syndrome: long-term follow-up and genetic heterogeneity.
    Jung C; Dagoneau N; Baujat G; Le Merrer M; David A; Di Rocco M; Hamel B; Mégarbané A; Superti-Furga A; Unger S; Munnich A; Cormier-Daire V
    Clin Genet; 2010 Mar; 77(3):266-72. PubMed ID: 20447141
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 185(3):856-865. PubMed ID: 33305909
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Effects of leukemia inhibitory receptor gene mutations on human hypothalamo-pituitary-adrenal function.
    Guran T; Guran O; Paketci C; Kipoglu O; Firat I; Turan S; Atay Z; Haliloglu B; Bereket A
    Pituitary; 2015 Aug; 18(4):456-60. PubMed ID: 25145448
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rhabdomyolysis in Stuve-Wiedemann syndrome.
    Ramdeny PS; Powell C; Chakraborty M; Hartley L
    BMJ Case Rep; 2018 Feb; 2018():. PubMed ID: 29437806
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Stüve-Wiedemann syndrome and related bent bone dysplasias.
    Akawi NA; Ali BR; Al-Gazali L
    Clin Genet; 2012 Jul; 82(1):12-21. PubMed ID: 22300393
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Paediatric survivors beyond infancy with Stüve-Wiedemann syndrome - A case series from the West Midlands, UK.
    McDermott H; Simmonds J; Thyagarajan M; ; Islam L; Naik S; Titheradge H
    Eur J Med Genet; 2023 Aug; 66(8):104788. PubMed ID: 37295610
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Anesthesia for Stüve-Wiedemann syndrome: a rare adult patient case report.
    Artilheiro V; Portela F; Reis AT
    J Appl Genet; 2020 Dec; 61(4):571-573. PubMed ID: 32910413
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Long-term follow-up in Stuve-Wiedemann syndrome: a clinical report.
    Gaspar IM; Saldanha T; Cabral P; Vilhena MM; Tuna M; Costa C; Dagoneau N; Daire VC; Hennekam RC
    Am J Med Genet A; 2008 Jul; 146A(13):1748-53. PubMed ID: 18546280
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Implications of neuropathy and management of the corneal surface in a patient with Stuve-Wiedemann syndrome.
    Cores ML; de Los Bueis AB
    Rom J Ophthalmol; 2023; 67(4):412-415. PubMed ID: 38239413
    [No Abstract]   [Full Text] [Related]  

  • 16. Stüve-Wiedemann syndrome with multiple eruptive vellus hair cysts and clefted tongue.
    Lobato-Berezo A; Tormo-Mainar S; Pujol RM
    Pediatr Dermatol; 2020 Mar; 37(2):381-382. PubMed ID: 31975458
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ocular treatment of children with Stuve-Wiedemann syndrome.
    Injarie AM; Narang A; Idrees Z; Saggar AK; Nischal KK
    Cornea; 2012 Mar; 31(3):269-72. PubMed ID: 22316651
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital bowing of the long bones in two fetuses presenting features of Stüve-Wiedemann syndrome and Schwartz-Jampel syndrome type 2.
    Sigaudy S; Moncla A; Fredouille C; Bourlière B; Lambert JC; Philip N
    Clin Dysmorphol; 1998 Oct; 7(4):257-62. PubMed ID: 9823491
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 38(5):553-8. PubMed ID: 21337444
    [TBL] [Abstract][Full Text] [Related]  

  • 20. EXT-related pathways are not involved in the pathogenesis of dysplasia epiphysealis hemimelica and metachondromatosis.
    Bovée JV; Hameetman L; Kroon HM; Aigner T; Hogendoorn PC
    J Pathol; 2006 Jul; 209(3):411-9. PubMed ID: 16622899
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.