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 *

143 related articles for article (PubMed ID: 38914824)

  • 41. Introduction: hereditary hemorrhagic telangiectasia as a rare disease.
    Daina E; D'Ovidio F; Sabbà C
    Curr Pharm Des; 2006; 12(10):1171-2. PubMed ID: 16611098
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Outcome of over 1500 matches through the Matchmaker Exchange for rare disease gene discovery: The 2-year experience of Care4Rare Canada.
    Osmond M; Hartley T; Dyment DA; Kernohan KD; Brudno M; Buske OJ; Innes AM; Boycott KM;
    Genet Med; 2022 Jan; 24(1):100-108. PubMed ID: 34906465
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Patient's perspective about research landscape for rare diseases in India.
    Kapadia A
    J Biosci; 2024; 49():. PubMed ID: 38383970
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Model network: Canadian program aims to generate models for rare disease.
    Foley KE
    Nat Med; 2015 Nov; 21(11):1242-3. PubMed ID: 26540381
    [No Abstract]   [Full Text] [Related]  

  • 45. Rare diseases in Romania - a response to 'transposition and implementation of EU rare diseases policy in Eastern Europe'.
    Severin E
    Expert Rev Pharmacoecon Outcomes Res; 2018 Jun; 18(3):233-234. PubMed ID: 29683365
    [No Abstract]   [Full Text] [Related]  

  • 46. Recent Developments in Using
    Oriel C; Lasko P
    Int J Mol Sci; 2018 Jul; 19(7):. PubMed ID: 30011838
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Authors' reply to Rare diseases in Romania - a response to 'Transposition and implementation of EU rare diseases policy in Eastern Europe'.
    Pejcic AV; Iskrov G; Stefanov R
    Expert Rev Pharmacoecon Outcomes Res; 2018 Aug; 18(4):349-350. PubMed ID: 29923755
    [No Abstract]   [Full Text] [Related]  

  • 48. Living with a rare disease - experiences and needs in pediatric patients and their parents.
    Witt S; Schuett K; Wiegand-Grefe S; Boettcher J; Quitmann J
    Orphanet J Rare Dis; 2023 Aug; 18(1):242. PubMed ID: 37568186
    [TBL] [Abstract][Full Text] [Related]  

  • 49. CPMS-improving patient care in Europe via virtual case discussions.
    Mönig I; Steenvoorden D; de Graaf JP; Ahmed SF; Taruscio D; Beun JG; Johannsen TH; Juul A; Hiort O; Pereira AM
    Endocrine; 2021 Mar; 71(3):549-554. PubMed ID: 33528763
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Rare Disease Biospecimens and Patient Registries: Interoperability for Research Promotion, a European Example: EuroBioBank and SpainRDR-BioNER.
    Rubinstein YR; Posada de la Paz M; Mora M
    Adv Exp Med Biol; 2017; 1031():141-147. PubMed ID: 29214569
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Phenotypic similarity-based approach for variant prioritization for unsolved rare disease: a preliminary methodological report.
    Lagorce D; Lebreton E; Matalonga L; Hongnat O; Chahdil M; Piscia D; Paramonov I; Ellwanger K; Köhler S; Robinson P; Graessner H; Beltran S; Lucano C; Hanauer M; Rath A
    Eur J Hum Genet; 2024 Feb; 32(2):182-189. PubMed ID: 37926714
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Where are we now in the investigation of rare diseases in the Republic of Macedonia?
    Polenakovic M; Gucev Z; Tasic V
    Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2014; 35(1):85-6. PubMed ID: 24798597
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Harmonising phenomics information for a better interoperability in the rare disease field.
    Maiella S; Olry A; Hanauer M; Lanneau V; Lourghi H; Donadille B; Rodwell C; Köhler S; Seelow D; Jupp S; Parkinson H; Groza T; Brudno M; Robinson PN; Rath A
    Eur J Med Genet; 2018 Nov; 61(11):706-714. PubMed ID: 29425702
    [TBL] [Abstract][Full Text] [Related]  

  • 54. The Occurrence of 275 Rare Diseases and 47 Rare Disease Groups in Italy. Results from the National Registry of Rare Diseases.
    Taruscio D; Vittozzi L; Rocchetti A; Torreri P; Ferrari L
    Int J Environ Res Public Health; 2018 Jul; 15(7):. PubMed ID: 30002291
    [TBL] [Abstract][Full Text] [Related]  

  • 55. ERN BOND: The key European network leveraging diagnosis, research, and treatment for rare bone conditions.
    Casareto L; Appelman-Dijkstra NM; Brandi ML; Chapurlat R; Cormier-Daire V; Hamdy NAT; Heath KE; Horn J; Mantovani G; Mohnike K; Sousa SB; Travessa A; Wekre LL; Zillikens MC; Sangiorgi L;
    Eur J Med Genet; 2024 Apr; 68():104916. PubMed ID: 38296035
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Conception of an Expert Advisory Board for the European Reference Network for Rare Respiratory Diseases.
    Walther D; Steinmann O; Schaefer J; Wagner TOF; Storf H
    Stud Health Technol Inform; 2018; 247():236-240. PubMed ID: 29677958
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Research data mismanagement - from questionable research practice to research misconduct.
    Yeo-Teh NSL; Tang BL
    Account Res; 2024 Aug; 31(6):706-713. PubMed ID: 36511716
    [TBL] [Abstract][Full Text] [Related]  

  • 58. The context for the thematic grouping of rare diseases to facilitate the establishment of European Reference Networks.
    Evangelista T; Hedley V; Atalaia A; Johnson M; Lynn S; Le Cam Y; Bushby K
    Orphanet J Rare Dis; 2016 Feb; 11():17. PubMed ID: 26911987
    [TBL] [Abstract][Full Text] [Related]  

  • 59. From gene to treatment: supporting rare disease translational research through model systems.
    Hmeljak J; Justice MJ
    Dis Model Mech; 2019 Feb; 12(2):. PubMed ID: 30819728
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN).
    Félix TM; de Oliveira BM; Artifon M; Carvalho I; Bernardi FA; Schwartz IVD; Saute JA; Ferraz VEF; Acosta AX; Sorte NB; Alves D;
    Orphanet J Rare Dis; 2022 Feb; 17(1):84. PubMed ID: 35209917
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.