Novel IL-12Rβ1 Deficiency Mediated Recurrent Cutaneous Leishmaniasis

Mendelian susceptibility to mycobacterial disease: recent discoveries

(2020) Jacinta Bustamante   HUMAN GENETICS

The Geographical Distribution of Cutaneous Leishmaniasis Causative Agents in Iran and Its Neighboring Countries, A Review

(2020) Mohammad Amin Ghatee et al.   Frontiers in Public Health

Mechanism-Based Precision Therapy for the Treatment of Primary Immunodeficiency and Primary Immunodysregulatory Diseases

(2019) Jennifer W. Leiding et al.   Journal of Allergy and Clinical Immunology-In Practice

Novel nonsense IL-12Rβ1 mutation associated with recurrent tuberculosis

(2019) Noor ul Akbar et al.   IMMUNOLOGIC RESEARCH

Leishmaniasis

(2018) Sakib Burza et al.   LANCET

Paracoccidioidomycosis Associated With a Heterozygous STAT4 Mutation and Impaired IFN-γ Immunity

(2017) Lena F Schimke et al.   JOURNAL OF INFECTIOUS DISEASES

Revisiting antithrombotic therapeutics; sculptin, a novel specific, competitive, reversible, scissile and tight binding inhibitor of thrombin

(2017) Asif Iqbal et al.   Scientific Reports

Cutaneous Leishmaniasis in Khyber Pakhtunkhwa Province of Pakistan: Clinical Diversity and Species-Level Diagnosis

(2016) Nazma Habib Khan et al.   AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE

Exome and genome sequencing for inborn errors of immunity

(2016) Isabelle Meyts et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Visceral Leishmaniasis May Unmask X-linked Hyper-IgM Syndrome

(2016) Luis Ignacio Gonzalez-Granado et al.   JOURNAL OF CLINICAL IMMUNOLOGY

Visceral leishmaniasis in two patients with IL-12p40 and IL-12Rβ1 deficiencies

(2016) Nima Parvaneh et al.   PEDIATRIC BLOOD & CANCER

Clinical and genetic features of il12rb1 deficiency: single center experience of 18 patients

(2016) Çağman Tan et al.   TURKISH JOURNAL OF PEDIATRICS

The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis

(2015) S. F. Bode et al.   HAEMATOLOGICA

The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis

(2015) S. F. Bode et al.   HAEMATOLOGICA

Mendelian susceptibility to mycobacterial disease: Genetic, immunological, and clinical features of inborn errors of IFN-γ immunity

(2014) Jacinta Bustamante et al.   SEMINARS IN IMMUNOLOGY

IL-12Rβ1 Deficiency: Mutation Update and Description of theIL12RB1Variation Database

(2013) Esther van de Vosse et al.   HUMAN MUTATION

Inherited human OX40 deficiency underlying classic Kaposi sarcoma of childhood

(2013) Minji Byun et al.   JOURNAL OF EXPERIMENTAL MEDICINE

Innate Defects of the IL-12/IFN-γ Axis in Susceptibility to Infections by Mycobacteria and Salmonella

(2013) Noé Ramirez-Alejo et al.   JOURNAL OF INTERFERON AND CYTOKINE RESEARCH

Inherited IL-12p40 Deficiency

(2013) Carolina Prando et al.   MEDICINE

Leishmaniasis Worldwide and Global Estimates of Its Incidence

(2012) Jorge Alvar et al.   PLoS One

Visceral Leishmaniasis as a Cause of Persistent Fever in Pediatric Hodgkin Lymphoma

(2011) Chinmaya Kumar Pani et al.   PEDIATRIC INFECTIOUS DISEASE JOURNAL

IL-12Rβ1 Deficiency in Two of Fifty Children with Severe Tuberculosis from Iran, Morocco, and Turkey

(2011) Stéphanie Boisson-Dupuis et al.   PLoS One

Crystal Structure of the Entire Ectodomain of gp130

(2010) Yibin Xu et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Revisiting Human IL-12Rβ1 Deficiency

(2010) Ludovic de Beaucoudrey et al.   MEDICINE

VISCERAL LEISHMANIASIS ASSOCIATED HEMOPHAGOCYTIC SYNDROME IN PATIENTS WITH CHRONIC GRANULOMATOUS DISEASE

(2010) Andrea Martín et al.   PEDIATRIC INFECTIOUS DISEASE JOURNAL