BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

282 related articles for article (PubMed ID: 24618404)

  • 21. 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; 52(4):242-6. PubMed ID: 19371797
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Non-truncating LIFR mutation: causal for prominent congenital pain insensitivity phenotype with progressive vertebral destruction?
    Elsaid MF; Chalhoub N; Kamel H; Ehlayel M; Ibrahim N; Elsaid A; Kumar P; Khalak H; Ilyin VA; Suhre K; Abdel Aleem A
    Clin Genet; 2016 Feb; 89(2):210-6. PubMed ID: 26285796
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Neuroparalytic keratopathy in Stüve-Wiedemann syndrome treated with tarsoconjunctival flap.
    Hernández-García S; Valdivia HG; Bartomeu JP; Molina JS
    Indian J Ophthalmol; 2023 Apr; 71(4):1651-1653. PubMed ID: 37026318
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mutations in the leukemia inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformations.
    Kosfeld A; Brand F; Weiss AC; Kreuzer M; Goerk M; Martens H; Schubert S; Schäfer AK; Riehmer V; Hennies I; Bräsen JH; Pape L; Amann K; Krogvold L; Bjerre A; Daniel C; Kispert A; Haffner D; Weber RG
    Hum Mol Genet; 2017 May; 26(9):1716-1731. PubMed ID: 28334964
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. One in three: congenital bent bone disease and intermittent hyperthermia in three siblings with stuve-wiedemann syndrome.
    Koul R; Al-Kindy A; Mani R; Sankhla D; Al-Futaisi A
    Sultan Qaboos Univ Med J; 2013 May; 13(2):301-5. PubMed ID: 23862038
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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; 78(2):146-9. PubMed ID: 9674905
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. 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]  

  • 32. 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]  

  • 33. Absence of GP130 cytokine receptor signaling causes extended Stüve-Wiedemann syndrome.
    Chen YH; Grigelioniene G; Newton PT; Gullander J; Elfving M; Hammarsjö A; Batkovskyte D; Alsaif HS; Kurdi WIY; Abdulwahab F; Shanmugasundaram V; Devey L; Bacrot S; Brodszki J; Huber C; Hamel B; Gisselsson D; Papadogiannakis N; Jedrycha K; Gürtl-Lackner B; Chagin AS; Nishimura G; Aschenbrenner D; Alkuraya FS; Laurence A; Cormier-Daire V; Uhlig HH
    J Exp Med; 2020 Mar; 217(3):. PubMed ID: 31914175
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Bilateral giant retinal tears in a pediatric patient with leukemia inhibitory factor receptor deficiency (Stuve-Wiedemann syndrome).
    Palejwala NV; Stempel AJ; Stout JT
    Retin Cases Brief Rep; 2015; 9(3):245-7. PubMed ID: 25876185
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel termination site in a case of Stüve-Wiedemann syndrome: case report and review of literature.
    Bhalla D; Sati S; Basel D; Karody V
    Front Pediatr; 2024; 12():1341841. PubMed ID: 38628360
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Case Report: Stüve-Wiedemann syndrome-a rare cause of persistent pulmonary hypertension of the newborn.
    Jin J; Rothämel P; Büchel J; Kammer B; Brunet T; Pattathu J; Flemmer AW; Nussbaum C; Schroepf S
    Front Pediatr; 2023; 11():1329404. PubMed ID: 38239591
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Clinical overview and outcome of the Stuve-Wiedemann syndrome: a systematic review.
    Warnier H; Barrea C; Bethlen S; Schrouff I; Harvengt J
    Orphanet J Rare Dis; 2022 Apr; 17(1):174. PubMed ID: 35461249
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Opposing Roles of Acetylation and Phosphorylation in LIFR-Dependent Self-Renewal Growth Signaling in Mouse Embryonic Stem Cells.
    Wang XJ; Qiao Y; Xiao MM; Wang L; Chen J; Lv W; Xu L; Li Y; Wang Y; Tan MD; Huang C; Li J; Zhao TC; Hou Z; Jing N; Chin YE
    Cell Rep; 2017 Jan; 18(4):933-946. PubMed ID: 28122243
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Exercise rescued chronic kidney disease by attenuating cardiac hypertrophy through the cardiotrophin-1 -> LIFR/gp 130 -> JAK/STAT3 pathway.
    Chen KC; Hsieh CL; Peng CC; Peng RY
    Eur J Prev Cardiol; 2014 Apr; 21(4):507-20. PubMed ID: 23064267
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Contributions of leukemia inhibitory factor receptor and oncostatin M receptor to signal transduction in heterodimeric complexes with glycoprotein 130.
    Hermanns HM; Radtke S; Haan C; Schmitz-Van de Leur H; Tavernier J; Heinrich PC; Behrmann I
    J Immunol; 1999 Dec; 163(12):6651-8. PubMed ID: 10586060
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.