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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1958 1
1959 1
1960 3
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1962 7
1963 5
1964 6
1965 6
1966 12
1967 14
1968 19
1969 17
1970 19
1971 24
1972 36
1973 34
1974 28
1975 40
1976 19
1977 26
1978 14
1979 19
1980 20
1981 13
1982 12
1983 23
1984 20
1985 16
1986 23
1987 21
1988 23
1989 27
1990 28
1991 27
1992 29
1993 41
1994 20
1995 41
1996 40
1997 40
1998 56
1999 83
2000 94
2001 120
2002 107
2003 116
2004 143
2005 128
2006 126
2007 163
2008 131
2009 152
2010 144
2011 154
2012 143
2013 179
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2015 149
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2017 138
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2019 100
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2021 119
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2023 98
2024 70

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3,849 results

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Page 1
Wiskott-Aldrich syndrome: a comprehensive review.
Massaad MJ, Ramesh N, Geha RS. Massaad MJ, et al. Ann N Y Acad Sci. 2013 May;1285:26-43. doi: 10.1111/nyas.12049. Epub 2013 Mar 25. Ann N Y Acad Sci. 2013. PMID: 23527602 Review.
Wiskott-Aldrich syndrome (WAS) is a rare X-linked primary immunodeficiency characterized by microthrombocytopenia, eczema, recurrent infections, and an increased incidence of autoimmunity and malignancies. ...
Wiskott-Aldrich syndrome (WAS) is a rare X-linked primary immunodeficiency characterized by microthrombocytopenia, ecze …
How I manage patients with Wiskott Aldrich syndrome.
Rivers E, Worth A, Thrasher AJ, Burns SO. Rivers E, et al. Br J Haematol. 2019 May;185(4):647-655. doi: 10.1111/bjh.15831. Epub 2019 Mar 12. Br J Haematol. 2019. PMID: 30864154 Free PMC article. Review.
Wiskott Aldrich syndrome (WAS) is a primary immunodeficiency disease resulting in recurrent infections, eczema and microthrombocytopaenia. ...
Wiskott Aldrich syndrome (WAS) is a primary immunodeficiency disease resulting in recurrent infections, eczema and micr …
Wiskott-Aldrich syndrome.
Notarangelo LD, Miao CH, Ochs HD. Notarangelo LD, et al. Curr Opin Hematol. 2008 Jan;15(1):30-6. doi: 10.1097/MOH.0b013e3282f30448. Curr Opin Hematol. 2008. PMID: 18043243 Review.
PURPOSE OF REVIEW: Wiskott-Aldrich syndrome is caused by mutations of the Wiskott-Aldrich syndrome protein gene, which codes for a cytoplasmic protein with multiple functions. ...The discovery of unique functional domains of Wiskott …
PURPOSE OF REVIEW: Wiskott-Aldrich syndrome is caused by mutations of the Wiskott-Aldrich syndrome …
Wiskott-Aldrich syndrome.
Nonoyama S, Ochs HD. Nonoyama S, et al. Curr Allergy Asthma Rep. 2001 Sep;1(5):430-7. doi: 10.1007/s11882-001-0028-0. Curr Allergy Asthma Rep. 2001. PMID: 11892069 Review.
Wiskott-Aldrich syndrome (WAS) is an X-linked immunodeficiency characterized by thrombocytopenia with small platelets, eczema, recurrent infections, autoimmune disorders, IgA nephropathy, and an increased incidence of hematopoietic malignancies. The identific …
Wiskott-Aldrich syndrome (WAS) is an X-linked immunodeficiency characterized by thrombocytopenia with small platelets, …
The Wiskott-Aldrich syndrome.
Ochs HD, Thrasher AJ. Ochs HD, et al. J Allergy Clin Immunol. 2006 Apr;117(4):725-38; quiz 739. doi: 10.1016/j.jaci.2006.02.005. J Allergy Clin Immunol. 2006. PMID: 16630926 Review.
The Wiskott-Aldrich syndrome (WAS) is a rare X-linked disorder with variable clinical phenotypes that correlate with the type of mutations in the WAS protein (WASP) gene. ...
The Wiskott-Aldrich syndrome (WAS) is a rare X-linked disorder with variable clinical phenotypes that correlate with th …
The Wiskott-Aldrich syndrome.
Orange JS, Stone KD, Turvey SE, Krzewski K. Orange JS, et al. Cell Mol Life Sci. 2004 Sep;61(18):2361-85. doi: 10.1007/s00018-004-4086-z. Cell Mol Life Sci. 2004. PMID: 15378206 Free PMC article. Review.
The Wiskott-Aldrich Syndrome (WAS) is an inherited immunodeficiency caused by a variety of mutations in the gene encoding the WAS protein (WASp). ...
The Wiskott-Aldrich Syndrome (WAS) is an inherited immunodeficiency caused by a variety of mutations in the gene encodi …
Gene therapy for Wiskott-Aldrich Syndrome.
Bosticardo M, Ferrua F, Cavazzana M, Aiuti A. Bosticardo M, et al. Curr Gene Ther. 2014;14(6):413-21. doi: 10.2174/1566523214666140918103731. Curr Gene Ther. 2014. PMID: 25245089 Review.
The Wiskott-Aldrich Syndrome (WAS) is a monogenic X-linked primary immunodeficiency characterised also by thrombocytopenia, eczema, and a high susceptibility to develop tumours and autoimmunity. ...
The Wiskott-Aldrich Syndrome (WAS) is a monogenic X-linked primary immunodeficiency characterised also by thrombocytope …
Diagnosis and clinical management of Wiskott-Aldrich syndrome: current and emerging techniques.
Cavannaugh C, Ochs HD, Buchbinder D. Cavannaugh C, et al. Expert Rev Clin Immunol. 2022 Jun;18(6):609-623. doi: 10.1080/1744666X.2022.2074400. Epub 2022 May 19. Expert Rev Clin Immunol. 2022. PMID: 35533396 Review.
INTRODUCTION: Wiskott-Aldrich syndrome (WAS) serves as the prototype of how variants in a gene, which encodes a protein central to actin cytoskeletal homeostasis can manifest clinically in a variety of ways including infection, atopy, autoimmunity, inflammati …
INTRODUCTION: Wiskott-Aldrich syndrome (WAS) serves as the prototype of how variants in a gene, which encodes a protein …
The Wiskott-Aldrich syndrome.
Ochs HD. Ochs HD. Isr Med Assoc J. 2002 May;4(5):379-84. Isr Med Assoc J. 2002. PMID: 12040832 Free article. Review. No abstract available.
3,849 results