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[Hereditary agammaglobulinemia (Bruton)].
1977
V Faber
Associated MeSH Terms
Cite
UI
MeSH Term
Description
Entries
D003937
Diagnosis, Differential
Determination of which one of two or more diseases or conditions a patient is suffering from by systematically comparing and contrasting results of diagnostic measures.
Diagnoses, Differential,Differential Diagnoses,Differential Diagnosis
D006801
Humans
Members of the species Homo sapiens.
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000361
Agammaglobulinemia
An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood.
Hypogammaglobulinemia,Agammaglobulinemias,Hypogammaglobulinemias
Related Publications
V Faber
Gene symbol: btk. Disease: Bruton agammaglobulinemia.
September 2003, Human genetics,
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[2 cases of agammaglobulinemia type Bruton].
January 1967, Il Fracastoro,
V Faber
[X-linked Bruton congenital agammaglobulinemia. Case report].
January 2009, Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi,
V Faber
Bruton tyrosine kinase (BTK) in X-linked agammaglobulinemia (XLA).
December 2000, Frontiers in bioscience : a journal and virtual library,
V Faber
Atypical course of COVID-19 in patient with Bruton agammaglobulinemia.
November 2020, Journal of infection in developing countries,
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Presentation of a case of Bruton type primary agammaglobulinemia in Guinea.
January 2020, The Pan African medical journal,
V Faber
[Intrathecal interferon therapy in chronic echovirus meningoencephalitis in Bruton type agammaglobulinemia].
January 1998, Klinische Padiatrie,
V Faber
Agammaglobulinemia, by Col. Ogden C. Bruton, MC, USA, Pediatrics, 1952;9:722-728.
July 1998, Pediatrics,
V Faber
Bruton-type (congenital X-linked) agammaglobulinemia: MR imaging of unusual intracranial complications.
January 1992, AJNR. American journal of neuroradiology,
V Faber
Novel insertions of Bruton tyrosine kinase in patients with X-linked agammaglobulinemia.
December 2002, Human mutation,
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