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Collection : Lilloa (Hal Lille Open Archive, Universite De Lille) Language : catalan; valencian Language : english Language : greek Publisher : biomed central
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Academic Journal

Comparative analysis of response to treatments and molecular features of tumor-derived organoids versus cell lines and PDX derived from the same ovarian clear cell carcinoma.

  • Authors :

Subjects: [SDV]Life Sciences [q-bio]

  • Source: ISSN: 1756-9966 ; Journal of experimental & clinical cancer research ; https://hal.univ-lille.fr/hal-04419676 ; Journal of experimental & clinical cancer research, 2023, Journal of Experimental &

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Academic Journal

Attenuated androgen discontinuation in patients with hereditary angioedema: a commented case series.

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Subjects: Angioedema;

  • Source: ISSN: 1710-1484.

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    Academic Journal

    Impact of methodological choices in comparative effectiveness studies: application in natalizumab versus fingolimod comparison among patients with multiple sclerosis

    • Authors :

    Subjects: Causal contrasts;

  • Source: ISSN: 1471-2288 ; BMC Medical Research Methodology ; https://univ-rennes.hal.science/hal-03690493 ; BMC Medical Research Methodology, 2022, 22 (1), pp.155. ⟨10.1186/s12874-022-01623-8⟩.

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    Academic Journal

    Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)

    • Authors :

    Subjects: Type 2 familial partial lipodystrophy;

  • Source: ISSN: 1750-1172 ; Orphanet Journal of Rare Diseases ; https://hal.sorbonne-universite.fr/hal-03649738 ; Orphanet Journal of Rare Diseases, 2022, ⟨10.1186/s13023-022-02308-7⟩.

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    Longitudinal assessment of systemic steroid therapy on hyperinflammatory endothelial biomarker profiles and serology responses of COVID-19 patients

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    Subjects: COVID-19;

  • Source: EISSN: 1479-5876 ; Journal of Translational Medicine ; https://hal.science/hal-04354174 ; Journal of Translational Medicine, 2022, 20 (1), pp.411. ⟨10.1186/s12967-022-03583-5⟩

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    Academic Journal

    Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.

    • Authors :

    Subjects: Gene families;

  • Source: ISSN: 1756-994X ; Genome Medicine ; https://hal.univ-lille.fr/hal-04219731 ; Genome Medicine, 2021, Genome Medicine, 13 (63), ⟨10.1186/s13073-021-00870-6⟩.

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    Academic Journal

    Serum transferrin as a biomarker of hepatocyte nuclear factor 4 alpha activity and hepatocyte function in liver diseases

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    Subjects: End-stage liver disease;

  • Source: ISSN: 1741-7015.

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    Academic Journal

    Iron status influences non-alcoholic fatty liver disease in obesity through the gut microbiome

    • Authors :

    Subjects: Ferritin;

  • Source: EISSN: 2049-2618 ; Microbiome ; https://cnrs.hal.science/hal-03451206 ; Microbiome, 2021, 9, ⟨10.1186/s40168-021-01052-7⟩

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    Academic Journal

    Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

    • Authors :

    Subjects: Genetic association studies Mendelian randomisation LDL-cholesterol Phenome-wide association scan;

  • Source: ISSN: 1471-2261 ; BMC Cardiovascular Disorders ; https://hal.sorbonne-universite.fr/hal-04479637 ; BMC Cardiovascular Disorders, 2019, 19, ⟨10.1186/s12872-019-1187-z⟩.

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    Academic Journal

    Raising rare disease awareness using red flags, role play simulation and patient educators: results of a novel educational workshop on Raynaud phenomenon and systemic sclerosis

    • Authors :

    Subjects: [SDV]Life Sciences [q-bio]

    • Source: ISSN: 1750-1172 ; Orphanet Journal of Rare Diseases ; https://hal.science/hal-02880743 ; Orphanet Journal of Rare Diseases, 2020, 15 (1), ⟨10.1186/s13023-020-01439-z⟩.

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    • 1-10 of  38 results for ""A., H.""