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Results for
""Agammaglobulinemia""[mesh_terms]

21 Results

Searching titles within these results

The Rapidly Expanding Genetic Spectrum of Common Variable Immunodeficiency-Like Disorders.

Rohan Ameratunga, Emily S J Edwards, Klaus Lehnert, Euphemia Leung, See-Tarn Woon, Edward Lea, Caroline Allan, Lydia Chan, Richard Steele, Hilary Longhurst, Vanessa L Bryant

The journal of allergy and clinical immunology. In practice 2023;11(6):1646-1664

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Eosinophilic Gastrointestinal Diseases.

Irene Mikhail, Hugh Sampson

The journal of allergy and clinical immunology. In practice 2016;4(2):369-70; quiz 371

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Role of rare immune cells in common variable immunodeficiency.

Hassan Abolhassani, Mojdeh Soltani, Mahnaz Rezaei, Saba Fekrvand, Mazdak Ganjalikhani-Hakemi, Reza Yazdani

Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2022;33(2):e13725

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Endogenous IgG hypogammaglobulinaemia in critically ill adults with sepsis: systematic review and meta-analysis.

Manu Shankar-Hari, Nicholas Culshaw, Benjamin Post, Eduardo Tamayo, David Andaluz-Ojeda, Jesús F Bermejo-Martín, Sebastian Dietz, Karl Werdan, Richard Beale, Jo Spencer, Mervyn Singer

Intensive care medicine 2016;41(8):1393-401

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Infant Botulism: Checklist for Timely Clinical Diagnosis and New Possible Risk Factors Originated from a Case Report and Literature Review.

Robertino Dilena, Mattia Pozzato, Lucia Baselli, Giovanna Chidini, Sergio Barbieri, Concetta Scalfaro, Guido Finazzi, Davide Lonati, Carlo Alessandro Locatelli, Alberto Cappellari, Fabrizio Anniballi

Toxins 2022;13(12):860

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BTKbase: the mutation database for X-linked agammaglobulinemia.

Jouni Väliaho, C I Edvard Smith, Mauno Vihinen

Human mutation 2006;27(12):1209-17

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Rare primary vasculitis: update on multiple complex diseases and the new kids on the block.

Frederico Augusto Gurgel Pinheiro, Joao Gabriel Dantas, Erika Biegelmeyer, Eduarda Bonelli Zarur

Advances in rheumatology (London, England) 2024;64(1):79

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Inborn errors of immunity and metabolic disorders: current understanding, diagnosis, and treatment approaches.

Pelin Teke Kisa, Nur Arslan

Journal of pediatric endocrinology & metabolism : JPEM 2021;34(3):277-294

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BTKbase, Bruton Tyrosine Kinase Variant Database in X-Linked Agammaglobulinemia: Looking Back and Ahead.

Gerard C P Schaafsma, Jouni Väliaho, Qing Wang, Anna Berglöf, Rula Zain, C I Edvard Smith, Mauno Vihinen

Human mutation 2025;2023():5797541

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Characterization of all possible single-nucleotide change caused amino acid substitutions in the kinase domain of Bruton tyrosine kinase.

Jouni Väliaho, Imrul Faisal, Csaba Ortutay, C I Edvard Smith, Mauno Vihinen

Human mutation 2016;36(6):638-47

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Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study.

Rosa Maria Dellepiane, Laura Dell'Era, Lorena Vanesa Beilis, Paola Pavesi, Micol Raimondi, Annarosa Soresina, Vassilios Lougaris, Maria Carrabba, Baldassarre Martire, Silvana Martino, Giovanna Russo, Giuseppe Patuzzo, Claudio Pignata, Giuseppe Spadaro, Romina Gallizzi, Marzia Duse, Fernando Giuseppe Specchia, Viviana Moschese, Gian Luigi Marseglia, Maria Cristina Pietrogrande, Giorgio Bedogni, Carlo Agostoni

Journal of clinical immunology 2016;35(7):595-7

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X-linked agammaglobulinemia associated with B-precursor acute lymphoblastic leukemia.

Akihiro Hoshino, Yusuke Okuno, Masahiro Migita, Hideki Ban, Xi Yang, Nobutaka Kiyokawa, Yuichi Adachi, Seiji Kojima, Osamu Ohara, Hirokazu Kanegane

Journal of clinical immunology 2015;35(2):108-11

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The efficacy of Pelargonium sidoides in the treatment of upper respiratory tract infections in children with transient hypogammaglobulinemia of infancy.

Turkan Patiroglu, Aydin Tunc, Hatice Eke Gungor, Ekrem Unal

Phytomedicine : international journal of phytotherapy and phytopharmacology 2014;19(11):958-61

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Adenosine deaminase type 2 deficiency masquerading as GATA2 deficiency: Successful hematopoietic stem cell transplantation.

Amy P Hsu, Robert R West, Katherine R Calvo, Jennifer Cuellar-Rodriguez, Mark Parta, Susan J Kelly, Nancy J Ganson, Michael S Hershfield, Steven M Holland, Dennis D Hickstein

The Journal of allergy and clinical immunology 2018;138(2):628-630.e2

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Gene therapy for PIDs: progress, pitfalls and prospects.

Adrian J Thrasher, Sayandip Mukherjee

Gene 2013;525(2):174-81

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Results: 1 – 15 / 21

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Results for ""Agammaglobulinemia""[mesh_terms]

The Rapidly Expanding Genetic Spectrum of Common Variable Immunodeficiency-Like Disorders.

Eosinophilic Gastrointestinal Diseases.

Role of rare immune cells in common variable immunodeficiency.

Endogenous IgG hypogammaglobulinaemia in critically ill adults with sepsis: systematic review and meta-analysis.

Infant Botulism: Checklist for Timely Clinical Diagnosis and New Possible Risk Factors Originated from a Case Report and Literature Review.

BTKbase: the mutation database for X-linked agammaglobulinemia.

Rare primary vasculitis: update on multiple complex diseases and the new kids on the block.

Inborn errors of immunity and metabolic disorders: current understanding, diagnosis, and treatment approaches.

BTKbase, Bruton Tyrosine Kinase Variant Database in X-Linked Agammaglobulinemia: Looking Back and Ahead.

Characterization of all possible single-nucleotide change caused amino acid substitutions in the kinase domain of Bruton tyrosine kinase.

Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study.

X-linked agammaglobulinemia associated with B-precursor acute lymphoblastic leukemia.

The efficacy of Pelargonium sidoides in the treatment of upper respiratory tract infections in children with transient hypogammaglobulinemia of infancy.

Adenosine deaminase type 2 deficiency masquerading as GATA2 deficiency: Successful hematopoietic stem cell transplantation.

Gene therapy for PIDs: progress, pitfalls and prospects.

Results for
""Agammaglobulinemia""[mesh_terms]