Disease: Mendelian susceptibility to atypical mycobacteria
- A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial Disease
- A Syrian Refugee in Iraq Diagnosed as a Case of IL12RB1 Deficiency in Japan Using Dried Blood Spots
- Clinical and Molecular Findings in Mendelian Susceptibility to Mycobacterial Diseases: Experience From India
- Diagnosis and Management of Infections in Patients with Mendelian Susceptibility to Mycobacterial Disease
- Diagnostic and therapeutic challenges in a child with complete interferon-γ receptor 1 deficiency
- Different penetrance of disseminated infections caused by nontuberculous Mycobacteria in Mendelian susceptibility to mycobacterial disease associated with a novel mutation
- Disseminated Bacillus Calmette-Guérin Osteomyelitis in Twin Sisters Related to STAT1 Gene Deficiency
- Disseminated Mycobacterium avium complex infection in a child with partial dominant interferon gamma receptor 1 deficiency in India
- Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature
- Family relationship, water contact and occurrence of Buruli ulcer in Benin
- First Association of Interleukin 12 Receptor Beta 1 Deficiency with Sjögren's Syndrome
- Genetic heterogeneity of Mendelian susceptibility to mycobacterial infection
- Genetic lessons learned from X-linked Mendelian susceptibility to mycobacterial diseases
- Genetic predisposition to infective diseases in humans. Mendelian predisposition to mycobacterial infections
- Genetics and immunity of tuberculosis
- Human host genetic factors in nontuberculous mycobacterial infection: lessons from single gene disorders affecting innate and adaptive immunity and lessons from molecular defects in interferon-gamma-dependent signaling
- IL12Rβ1 defect presenting with massive intra-abdominal lymphadenopathy due to Mycobacterium intracellulare infection
- Immune defects in active mycobacterial diseases in patients with primary immunodeficiency diseases (PIDs)
- Impact of molecular diagnosis on treating Mendelian susceptibility to mycobacterial diseases
- Impaired IL-12- and IL-23-Mediated Immunity Due to IL-12Rbeta1 Deficiency in Iranian Patients with Mendelian Susceptibility to Mycobacterial Disease
- Impaired IL-12- and IL-23-Mediated Immunity Due to IL-12Rβ1 Deficiency in Iranian Patients with Mendelian Susceptibility to Mycobacterial Disease
- Impaired interferon gamma-mediated immunity and susceptibility to mycobacterial infection in childhood
- Inherited disorders of IL-12- and IFNgamma-mediated immunity: a molecular genetics update
- Isolated mediastinal lymphadenitis caused by Mycobacterium malmoense in an immunocompromised child
- Manifestations of cutaneous mycobacterial infections in patients with inborn errors of IL-12/IL-23-IFNγ immunity
- Mendelian predisposition to mycobacterial infections in humans
- Mendelian susceptibility to mycobacterial disease in tuberculosis-hyperendemic South Africa
- Mendelian susceptibility to mycobacterial disease: a case report of disseminated infection due to Mycobacterium avium
- Mendelian susceptibility to mycobacterial disease: Clinical and immunological findings of patients suspected for IL12Rbeta1 deficiency
- Mendelian susceptibility to mycobacterial disease: Clinical and immunological findings of patients suspected for IL12Rβ1 deficiency
- Mendelian Susceptibility to Mycobacterial Disease: The First Case of a Diagnosed Adult Patient in the Czech Republic
- Mendelian Susceptibility to Mycobacterial Diseases (MSMD) in a 13-Year-Old Ethiopian Girl with Autosomal Dominant Interferon Gamma Receptor 1(IFN-<em>γ</em> R1) Defect: A Clinical Diagnostic and Treatment Challenge
- Mendelian Susceptibility to Mycobacterial Diseases (MSMD) in a 13-Year-Old Ethiopian Girl with Autosomal Dominant Interferon Gamma Receptor 1(IFN-gamma R1) Defect: A Clinical Diagnostic and Treatment Challenge
- Mendelian susceptibility to mycobacterial infection in man
- Mendelian susceptibility to mycobacterial infection in man
- Molecular, Immunological, and Clinical Features of 16 Iranian Patients with Mendelian Susceptibility to Mycobacterial Disease
- Multifocal infection due to Mycobacterium intracellulare: first case of interferon gamma receptor partial dominant deficiency in tropical French territory
- Mycobacterium bovis BCG-itis and cervical lymphadenitis due to Salmonella enteritidis in a patient with complete interleukin-12/-23 receptor beta1 deficiency
- NF-kappaB Essential Modulator Deficiency Leading to Disseminated Cutaneous Atypical Mycobacteria
- NF-κB Essential Modulator Deficiency Leading to Disseminated Cutaneous Atypical Mycobacteria
- Non-tuberculous mycobacteria in children: muddying the waters of tuberculosis diagnosis
- Non-tuberculous mycobacteriosis. What has been coming out
- Nontuberculous mycobacterial infections in children with inborn errors of the immune system
- Novel Mutation of Interferon-gamma Receptor 1 Gene Presenting as Early Life Mycobacterial Bronchial Disease
- Novel Mutation of Interferon-γ Receptor 1 Gene Presenting as Early Life Mycobacterial Bronchial Disease
- Novel STAT1 alleles in a patient with impaired resistance to mycobacteria
- Overview of nontuberculous mycobacterial disease in children
- Presentation of interleukin-12/-23 receptor beta1 deficiency with various clinical symptoms of Salmonella infections
- Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries
- Susceptibility to mycobacterial disease due to mutations in IL-12Rbeta1 in three Iranian patients
- Susceptibility to mycobacterial disease due to mutations in IL-12Rβ1 in three Iranian patients
- The Child with Recurrent Mycobacterial Disease
- Two siblings with an IL-12 and IFN-gamma production disorder diagnosed with pulmonary mycobacteriosis caused by M. kansasii. Mendelian susceptibility to mycobacterial infection: an overview of literature
- Two siblings with an IL-12 and IFN-γ production disorder diagnosed with pulmonary mycobacteriosis caused by M. kansasii. Mendelian susceptibility to mycobacterial infection: an overview of literature
- XDR TB in a case of IL12Rbeta1 deficiency: a case report of Mendelian Susceptibility to Mycobacterial Disease from India
- XDR TB in a case of IL12Rβ1 deficiency: a case report of Mendelian Susceptibility to Mycobacterial Disease from India