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Significados de wiskott-aldrich syndrome en inglés

ruso
синдром вискотта — олдрича
portugués
síndrome de wiskott-aldrich
español
sindrome de wiskott-aldrich

Rare disease.

      Términos relacionados
      sindrome de wiskott-aldrich
      Sinónimos
      Examples for "was"
      Examples for "was"
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      Some said later this year; others said 2020 was closer to reality.
      Wired
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      The problem was resolved within several weeks, The New York Times said.
      Reuters
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      He said a common sense approach to the Covid-19 situation was needed.
      Radio NZ
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      However, the jet's auxiliary power unit was able to continue supplying power.
      The Guardian
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      Now a new problem: There was no clear way to open it.
      Storm Front
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      Two patients with the Wiskott- Aldrich syndrome had complete donor lymphoid and hematopoietic engraftment after successful allogeneic bone-marrow transplantation.
      Pubmed
      2
      The Wiskott- Aldrich syndrome (WAS) is an X-linked recessive genetic disease in which the basic molecular defect is unknown.
      Pubmed
      3
      Background: Proliferation and IL-2 production in response to T-cell receptor ligation are impaired in patients with Wiskott- Aldrich syndrome (WAS).
      Pubmed
      4
      This treatment of the Wiskott- Aldrich syndrome may be a model for the correction of other genetically determined immune and hematologic bone-marrow disorders.
      Pubmed
      5
      The Wiskott- Aldrich syndrome is an X-linked hereditary disorder associated with combined immunodeficiency, thrombocytopenia, small platelets, eczema, and increased susceptibility to autoimmune disorders and cancers.
      Pubmed
      Uso de wiskott-aldrich syndrome en inglés
      1
      Two patients with the Wiskott-Aldrich syndrome had complete donor lymphoid and hematopoietic engraftment after successful allogeneic bone-marrow transplantation.
      Pubmed
      2
      The Wiskott-Aldrich syndrome (WAS) is an X-linked recessive genetic disease in which the basic molecular defect is unknown.
      Pubmed
      3
      Background: Proliferation and IL-2 production in response to T-cell receptor ligation are impaired in patients with Wiskott-Aldrich syndrome (WAS).
      Pubmed
      4
      This treatment of the Wiskott-Aldrich syndrome may be a model for the correction of other genetically determined immune and hematologic bone-marrow disorders.
      Pubmed
      5
      The Wiskott-Aldrich syndrome is an X-linked hereditary disorder associated with combined immunodeficiency, thrombocytopenia, small platelets, eczema, and increased susceptibility to autoimmune disorders and cancers.
      Pubmed
      6
      This mutation is likely to be the hypothesized genotype that caused the severe form of the Wiskott-Aldrich syndrome in the three brothers described by Wiskott.
      Pubmed
      7
      Here we establish a fluorescence resonance energy transfer-based approach to visualize spatial and temporal regulation of neuronal Wiskott-Aldrich syndrome protein (N-WASP) activity in living cells.
      Pubmed
      8
      The clinical data of 24 children with Wiskott-Aldrich syndrome (WAS) from 23 unrelated Chinese families were reviewed in the present study.
      Pubmed
      9
      Earlier observations of defective CD43 expression by T lymphocytes from boys with the X-chromosome-linked Wiskott-Aldrich syndrome suggested the importance of CD43 in lymphocyte function.
      Pubmed
      10
      A 28-year-old man with Wiskott-Aldrich syndrome presented with ulcerative-proliferative lesions on his face from which herpes simplex type 1 (HSV-1) was isolated.
      Pubmed
      Translations for wiskott-aldrich syndrome