BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 31837202)

  • 21. Myhre-LAPs syndrome and intubation related airway stenosis: keys to diagnosis and critical therapeutic interventions.
    Oldenburg MS; Frisch CD; Lindor NM; Edell ES; Kasperbauer JL; O'Brien EK
    Am J Otolaryngol; 2015; 36(5):636-41. PubMed ID: 25940662
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Myhre syndrome: Clinical features and restrictive cardiopulmonary complications.
    Starr LJ; Grange DK; Delaney JW; Yetman AT; Hammel JM; Sanmann JN; Perry DA; Schaefer GB; Olney AH
    Am J Med Genet A; 2015 Dec; 167A(12):2893-901. PubMed ID: 26420300
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Myhre syndrome with facial paralysis and branch pulmonary stenosis.
    Hawkes L; Kini U
    Clin Dysmorphol; 2015 Apr; 24(2):84-5. PubMed ID: 25486016
    [No Abstract]   [Full Text] [Related]  

  • 24. Bilateral otospongiosis and a unilateral vestibular schwannoma in a patient with Myhre syndrome.
    Kenis C; Verstreken M; Gieraerts K; De Foer B; Van der Aa N; Offeciers EF; Casselman JW
    Otol Neurotol; 2014 Oct; 35(9):e253-5. PubMed ID: 24841914
    [No Abstract]   [Full Text] [Related]  

  • 25. SMAD4 mutations causing Myhre syndrome result in disorganization of extracellular matrix improved by losartan.
    Piccolo P; Mithbaokar P; Sabatino V; Tolmie J; Melis D; Schiaffino MC; Filocamo M; Andria G; Brunetti-Pierri N
    Eur J Hum Genet; 2014 Aug; 22(8):988-94. PubMed ID: 24398790
    [TBL] [Abstract][Full Text] [Related]  

  • 26. SMAD4 mutations and cross-talk between TGF-β/IFNγ signaling accelerate rates of DNA damage and cellular senescence, resulting in a segmental progeroid syndrome-the Myhre syndrome.
    Kandhaya-Pillai R; Hou D; Zhang J; Yang X; Compoginis G; Mori T; Tchkonia T; Martin GM; Hisama FM; Kirkland JL; Oshima J
    Geroscience; 2021 Jun; 43(3):1481-1496. PubMed ID: 33428109
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Clinical features and respiratory complications in Myhre syndrome.
    McGowan R; Gulati R; McHenry P; Cooke A; Butler S; Keng WT; Murday V; Whiteford M; Dikkers FG; Sikkema-Raddatz B; van Essen T; Tolmie J
    Eur J Med Genet; 2011; 54(6):e553-9. PubMed ID: 21816239
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Myhre syndrome is caused by dominant-negative dysregulation of SMAD4 and other co-factors.
    Alankarage D; Enriquez A; Steiner RD; Raggio C; Higgins M; Milnes D; Humphreys DT; Duncan EL; Sparrow DB; Giampietro PF; Chapman G; Dunwoodie SL
    Differentiation; 2022; 128():1-12. PubMed ID: 36194927
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Myhre syndrome with ataxia and cerebellar atrophy.
    Bachmann-Gagescu R; Hisama FM; Yuen AL
    Clin Dysmorphol; 2011 Jul; 20(3):156-159. PubMed ID: 21490502
    [No Abstract]   [Full Text] [Related]  

  • 30. Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defects.
    Cappuccio G; Brunetti-Pierri N; Clift P; Learn C; Dykes JC; Mercer CL; Callewaert B; Meerschaut I; Spinelli AM; Bruno I; Gillespie MJ; Dorfman AT; Grimberg A; Lindsay ME; Lin AE
    Am J Med Genet A; 2022 May; 188(5):1384-1395. PubMed ID: 35025139
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Myhre syndrome: expanding its paediatric phenotypic spectrum.
    Brunet-Garcia L; Prada Martínez FH; Carretero Bellon JM
    Cardiol Young; 2023 Nov; 33(11):2408-2410. PubMed ID: 37325812
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3-4.
    Yang K; Wang X; Wang WQ; Han MY; Hu LM; Kang DY; Yang JY; Liu M; Gao X; Yuan YY; Xu JC
    Mol Genet Genomic Med; 2023 Mar; 11(3):e2103. PubMed ID: 36373990
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Autism Spectrum Disorder and Psychiatric Comorbidity in a Patient with Myhre Syndrome.
    Artemios P; Areti S; Katerina P; Helen F; Eirini T; Charalambos P
    J Autism Dev Disord; 2019 Jul; 49(7):3031-3035. PubMed ID: 30968316
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Multilevel Airway Stenosis Being Bypassed by a Customized Tracheostomy Tube in an Infant with Myhre Syndrome.
    Jeon MJ; Kim MJ; Kim JH; Park JS; Yim J; Kim M; Kwon SK; Lee S; Ko JM; Chae JH; Suh DI
    Pediatr Allergy Immunol Pulmonol; 2021 Jun; 34(2):83-87. PubMed ID: 34143683
    [No Abstract]   [Full Text] [Related]  

  • 35. Lack of resemblance between Myhre syndrome and other "segmental progeroid" syndromes warrants restraint in applying this classification.
    Lin AE; Brunetti-Pierri N; Callewaert B; Cormier-Daire V; Douzgou S; Kinane TB; Lindsay ME; Starr LJ;
    Geroscience; 2021 Apr; 43(2):459-461. PubMed ID: 33630210
    [No Abstract]   [Full Text] [Related]  

  • 36. Natural history of Myhre syndrome.
    Yang DD; Rio M; Michot C; Boddaert N; Yacoub W; Garcelon N; Thierry B; Bonnet D; Rondeau S; Herve D; Guey S; Angoulvant F; Cormier-Daire V
    Orphanet J Rare Dis; 2022 Jul; 17(1):304. PubMed ID: 35907855
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A pilot clinical trial with losartan in Myhre syndrome.
    Cappuccio G; Caiazza M; Roca A; Melis D; Iuliano A; Matyas G; Rubino M; Limongelli G; Brunetti-Pierri N
    Am J Med Genet A; 2021 Mar; 185(3):702-709. PubMed ID: 33369056
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Myhre Syndrome Misdiagnosed as Marfan Syndrome: an Educational Presentation.
    Li J; Zhu T; Yang S; Yang F; Wu J; Xiong F
    Braz J Cardiovasc Surg; 2021 Oct; 36(5):700-702. PubMed ID: 34236823
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Myhre syndrome: Age-dependent progressive phenotype.
    Nomura R; Miyai K; Nishimura G; Kashimada K; Morio T
    Pediatr Int; 2017 Nov; 59(11):1205-1206. PubMed ID: 29359479
    [No Abstract]   [Full Text] [Related]  

  • 40.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.