Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Immune deficiency syndromes"'
Publikováno v:
Медицинская иммунология, Vol 19, Iss 1, Pp 95-100 (2017)
The work represents a family which includes two siblings with chromosome 22q11.2 deletion syndrome. Their mother carries the same chromosome anomaly, but with apparently normal phenotype. Hence, this interesting case of 22q11.2 deletion syndrome exis
Externí odkaz:
https://doaj.org/article/37f763de45724cc993fe6fdefad04732
Publikováno v:
Medicine
In clinical practice, not all human immune deficiency virus (HIV) positive individuals who received highly active antiretroviral therapy (HAART) achieve the desired concordant response characterized by a sustained viral suppression or immune recovery
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52dbb06e3f0deb370a5fad91c29019e4
http://europepmc.org/articles/PMC8615327
http://europepmc.org/articles/PMC8615327
Publikováno v:
Jornal de Pediatria, Vol 95, Iss, Pp 49-58 (2019)
Jornal de Pediatria v.95 suppl.1 2019
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria, Volume: 95 Supplement 1, Pages: S49-S58, Published: 18 APR 2019
Jornal de Pediatria (Versão em Português), Vol 95, Iss, Pp 49-58 (2019)
Jornal de Pediatria v.95 suppl.1 2019
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria, Volume: 95 Supplement 1, Pages: S49-S58, Published: 18 APR 2019
Jornal de Pediatria (Versão em Português), Vol 95, Iss, Pp 49-58 (2019)
Objectives: This study aimed to review the literature on the repercussions of the different inborn errors of immunity on growth, drawing attention to the diagnosis of this group of diseases in patients with growth disorders, as well as to enable the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fabb801db9e18541860aad74427d202
http://www.sciencedirect.com/science/article/pii/S0021755718310726
http://www.sciencedirect.com/science/article/pii/S0021755718310726
Publikováno v:
Asia Pacific Allergy
Primary immunodeficiency disorders, although rare, pose a significant burden in the quality of life of afflicted patients and their families. The most common of these disorders are caused by B-cell defects. A total of 6 patients were seen and diagnos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9febba03fa13a0473f829fa398b52d4a
https://doi.org/10.5415/apallergy.2021.11.e7
https://doi.org/10.5415/apallergy.2021.11.e7
Akademický článek
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Publikováno v:
JAIDS: Journal of Acquired Immune Deficiency Syndromes. 12/15/2007, Vol. 46 Issue 5, p656-657. 2p.
Publikováno v:
JAIDS: Journal of Acquired Immune Deficiency Syndromes. 12/15/2007, Vol. 46 Issue 5, p657-658. 2p.
Publikováno v:
JAIDS: Journal of Acquired Immune Deficiency Syndromes. 12/15/2007, Vol. 46 Issue 5, p517-518. 2p.
Publikováno v:
Medical Immunology (Russia)
Медицинская иммунология
Медицинская иммунология
The work represents a family which includes two siblings with chromosome 22q11.2 deletion syndrome. Their mother carries the same chromosome anomaly, but with apparently normal phenotype. Hence, this interesting case of 22q11.2 deletion syndrome exis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______917::e35c251f9f11837d258e022903ce600e
http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85011015676
http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85011015676
