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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 31285900)

  • 21. Cost-effectiveness analysis of three algorithms for diagnosing primary ciliary dyskinesia: a simulation study.
    Kouis P; Papatheodorou SI; Middleton N; Giallouros G; Kyriacou K; Cohen JT; Evans JS; Yiallouros PK
    Orphanet J Rare Dis; 2019 Jun; 14(1):142. PubMed ID: 31196140
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Identification of a novel
    Kolkova Z; Durdik P; Holubekova V; Durdikova A; Jesenak M; Banovcin P
    Front Pediatr; 2024; 12():1339664. PubMed ID: 38333087
    [TBL] [Abstract][Full Text] [Related]  

  • 23.
    Cindrić S; Dougherty GW; Olbrich H; Hjeij R; Loges NT; Amirav I; Philipsen MC; Marthin JK; Nielsen KG; Sutharsan S; Raidt J; Werner C; Pennekamp P; Dworniczak B; Omran H
    Am J Respir Cell Mol Biol; 2020 Mar; 62(3):382-396. PubMed ID: 31545650
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Cilia ultrastructural and gene variation of primary ciliary dyskinesia: report of three cases and literatures review].
    Wang K; Chen X; Guo CY; Liu FQ; Wang JR; Sun LF
    Zhonghua Er Ke Za Zhi; 2018 Feb; 56(2):134-137. PubMed ID: 29429202
    [No Abstract]   [Full Text] [Related]  

  • 25. The Palestinian primary ciliary dyskinesia population: first results of the diagnostic and genetic spectrum.
    Rumman N; Fassad MR; Driessens C; Goggin P; Abdelrahman N; Adwan A; Albakri M; Chopra J; Doherty R; Fashho B; Freke GM; Hasaballah A; Jackson CL; Mohamed MA; Abu Nema R; Patel MP; Pengelly RJ; Qaaqour A; Rubbo B; Thomas NS; Thompson J; Walker WT; Wheway G; Mitchison HM; Lucas JS
    ERJ Open Res; 2023 Mar; 9(2):. PubMed ID: 37077557
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prevalence of chronic rhinosinusitis in bronchiectasis patients suspected of ciliary dyskinesia.
    McCormick JP; Weeks CG; Rivers NJ; Owen JD; Kelly DR; Rowe SM; Solomon GM; Woodworth BA; Cho DY
    Int Forum Allergy Rhinol; 2019 Dec; 9(12):1430-1435. PubMed ID: 31430425
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genotype and phenotype evaluation of patients with primary ciliary dyskinesia: First results from Turkey.
    Emiralioğlu N; Taşkıran EZ; Koşukcu C; Bilgiç E; Atilla P; Kaya B; Günaydın Ö; Yüzbaşıoğlu A; Tuğcu GD; Ademhan D; Eryılmaz Polat S; Gharibzadeh Hızal M; Yalçın E; Doğru D; Kiper N; Alikaşifoğlu M; Özçelik U
    Pediatr Pulmonol; 2020 Feb; 55(2):383-393. PubMed ID: 31765523
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Implementation of multigene panel NGS diagnosis in the national primary ciliary dyskinesia cohort of Cyprus: An island with a high disease prevalence.
    Yiallouros PK; Kouis P; Kyriacou K; Evriviadou A; Anagnostopoulou P; Matthaiou A; Tsiolakis I; Pirpa P; Michailidou K; Potamiti L; Loizidou MA; Hadjisavvas A
    Hum Mutat; 2021 Jun; 42(6):e62-e77. PubMed ID: 33715250
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry.
    Olbrich H; Schmidts M; Werner C; Onoufriadis A; Loges NT; Raidt J; Banki NF; Shoemark A; Burgoyne T; Al Turki S; Hurles ME; ; Köhler G; Schroeder J; Nürnberg G; Nürnberg P; Chung EM; Reinhardt R; Marthin JK; Nielsen KG; Mitchison HM; Omran H
    Am J Hum Genet; 2012 Oct; 91(4):672-84. PubMed ID: 23022101
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Primary ciliary dyskinesia with HYDIN gene mutations in a child and literature review].
    Chen LL; Yang YG; Wu JZ; Chen XR
    Zhonghua Er Ke Za Zhi; 2017 Apr; 55(4):304-307. PubMed ID: 28441829
    [No Abstract]   [Full Text] [Related]  

  • 31. Quantitative analysis of ciliary beating in primary ciliary dyskinesia: a pilot study.
    Papon JF; Bassinet L; Cariou-Patron G; Zerah-Lancner F; Vojtek AM; Blanchon S; Crestani B; Amselem S; Coste A; Housset B; Escudier E; Louis B
    Orphanet J Rare Dis; 2012 Oct; 7():78. PubMed ID: 23057704
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Heterozygous cis HYDIN mutations cause primary ciliary dyskinesia.
    Suryadinata R; Martinello P; Bennett-Wood V; Robinson P
    Med; 2024 Sep; ():. PubMed ID: 39317196
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Identification of a Novel
    Yang B; Lei C; Yang D; Lu C; Xu Y; Wang L; Guo T; Wang R; Luo H
    Pharmgenomics Pers Med; 2022; 15():697-704. PubMed ID: 35847568
    [TBL] [Abstract][Full Text] [Related]  

  • 34. CCDC40 mutation as a cause of primary ciliary dyskinesia: a case report and review of literature.
    Sui W; Hou X; Che W; Ou M; Sun G; Huang S; Liu F; Chen P; Wei X; Dai Y
    Clin Respir J; 2016 Sep; 10(5):614-21. PubMed ID: 25619595
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Whole-Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary Dyskinesia.
    Marshall CR; Scherer SW; Zariwala MA; Lau L; Paton TA; Stockley T; Jobling RK; Ray PN; Knowles MR; ; Hall DA; Dell SD; Kim RH
    G3 (Bethesda); 2015 Jul; 5(8):1775-81. PubMed ID: 26139845
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Case Report: Primary ciliary dyskinesia due to CCNO mutations: a Chinese pediatric case series and literature review.
    Tong L; Li L; Wang W; Chen J
    Front Pediatr; 2024; 12():1458660. PubMed ID: 39380637
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Clinical characteristics of primary ciliary dyskinesia in children].
    Xu BP; Shen KL; Hu YH; Feng XL; Li HM; Lang ZQ
    Zhonghua Er Ke Za Zhi; 2008 Aug; 46(8):618-22. PubMed ID: 19099837
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Pathogenic variants in
    Wohlgemuth K; Hoersting N; Koenig J; Loges NT; Raidt J; George S; Cindrić S; Schramm A; Biebach L; Lay S; Dougherty GW; Olbrich H; Pennekamp P; Dworniczak B; Omran H
    Eur Respir J; 2024 Oct; ():. PubMed ID: 39362668
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility.
    El Khouri E; Thomas L; Jeanson L; Bequignon E; Vallette B; Duquesnoy P; Montantin G; Copin B; Dastot-Le Moal F; Blanchon S; Papon JF; Lorès P; Yuan L; Collot N; Tissier S; Faucon C; Gacon G; Patrat C; Wolf JP; Dulioust E; Crestani B; Escudier E; Coste A; Legendre M; Touré A; Amselem S
    Am J Hum Genet; 2016 Aug; 99(2):489-500. PubMed ID: 27486783
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia.
    Raidt J; Wallmeier J; Hjeij R; Onnebrink JG; Pennekamp P; Loges NT; Olbrich H; Häffner K; Dougherty GW; Omran H; Werner C
    Eur Respir J; 2014 Dec; 44(6):1579-88. PubMed ID: 25186273
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.