Results 181 to 190 of about 12,870 (263)

A novel mutation in FNIP1 associated with a syndromic immunodeficiency and cardiomyopathy. [PDF]

Immunogenetics
Spivak I, Lev A, Simon AJ, Barel O, Somekh I, Somech R.   +5 more
europepmc   +1 more source

Gut microbial dysbiosis, IgA, and Enterococcus in common variable immunodeficiency with immune dysregulation. [PDF]

Microbiome
Berbers RM, Paganelli FL, van Montfrans JM, Ellerbroek PM, Viveen MC, Rogers MRC, Salomons M, Schuurmans J, van Stigt Thans M, Vanmaris RMM, Brosens LAA, van der Wal MM, Dalm VASH, van Hagen PM, van de Ven AAJM, Uh HW, van Wijk F, Willems RJL, Leavis HL.   +18 more
europepmc   +1 more source

Digenic Inheritance of Hereditary Spherocytosis Type III and X-linked Agammaglobulinemia: Coexistence of Two Distinct Recessive Disorders in a Male Child. [PDF]

Cureus
Almutairy KA, Alasmari BG, Rayees S.
europepmc   +1 more source

Abnormal T Cells Function Associated With Intraspinal Cold Abscess Caused by Macrolide-resistant Mycoplasma pneumoniae in a Patient With X-linked Agammaglobulinemia. [PDF]

Pediatr Infect Dis J
Jin YY, Wu J, Ding F, Huang H, Xu XM, Chen QM, Yin MZ, Zhong YM, Jin YL.   +8 more
europepmc   +1 more source

Carbapenem resistant Campylobacter jejuni bacteremia in a Bruton's X-linked agammaglobulinemia patient. [PDF]

Eur J Clin Microbiol Infect Dis
Zhuo R, Younes RL, Ward K, Yang S.
europepmc   +1 more source

Agammaglobulinemia ligada al cromosoma X, lo crucial del diagnóstico y tratamiento oportunos

, 2019
Dra Carla, Lucía Marcela López Vaca, Yépez Calle, Carla Lucía, Vaca Yépez, Jaira Hidalgo Vásconez   +5 more
openalex   +2 more sources

The dilemma of X-linked agammaglobulinemia carriers. [PDF]

J Allergy Clin Immunol Glob
Pulvirenti F, Milito C, Cinetto F, Garzi G, Sardella G, Spadaro G, Lippi F, Guarnieri V, Cinicola BL, Carrabba M, Guadagnolo D, Fabio G, Martire B, Cancrini C, Lanzoni G, Finocchi A, Di Matteo G, Pompilii E, Ferrari S, Quinti I.   +19 more
europepmc   +1 more source

Heterozygous deletion of 10q24.31-q24.33- a new syndrome associated with multiple congenital anomalies: case report and literature review. [PDF]

Neurol Res Pract
Buianova AA, Lashkova YS, Kulichenko TV, Kuznetsov IS, Ivanov AA, Parshina OP, Suchalko ON, Vakhlyarskaya SS, Korostin DO.   +8 more
europepmc   +1 more source

Neonatal Screening for Spinal Muscular Atrophy and Severe T- and B-Cell Lymphopenias in Andalusia: A Prospective Study. [PDF]

Int J Neonatal Screen
De Felipe B, Delgado-Pecellin C, Lopez-Lobato M, Olbrich P, Blanco-Lobo P, Marquez-Fernandez J, Salamanca C, Mendoza B, Castro-Serrano R, Duque C, Moreno-Prieto M, Madruga-Garrido M, Lucena JM, Fernandez RM, Ruiz-Camacho M, Varona A, Neth O.   +16 more
europepmc   +1 more source