| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Surjit Singh | |
| Amit Rawat | |||
| Dhrubajyoti Sharma | |||
| Ankur K Jindal | |||
| P2860 | cites work | Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment | Q24338530 |
| A Comprehensive Review of the Treatment of Atopic Eczema | Q26765975 | ||
| Systemic Lupus Erythematosus and Deficiencies of Early Components of the Complement Classical Pathway | Q26768534 | ||
| An update on the hyper-IgE syndromes | Q27021598 | ||
| Cancers Related to Immunodeficiencies: Update and Perspectives | Q28074182 | ||
| Primary immunodeficiency update: Part I. Syndromes associated with eczematous dermatitis | Q28086897 | ||
| Hyper-IgE syndromes: reviewing PGM3 deficiency | Q28250834 | ||
| Chediak-Higashi syndrome | Q28258929 | ||
| Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome | Q28266613 | ||
| Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity | Q28272650 | ||
| Population prevalence of diagnosed primary immunodeficiency diseases in the United States | Q28306873 | ||
| Autoimmunity in common variable immunodeficiency: epidemiology, pathophysiology and management. | Q30245322 | ||
| Autoimmunity in primary immune deficiency: taking lessons from our patients | Q33394794 | ||
| Wiskott-Aldrich syndrome: a comprehensive review | Q33406620 | ||
| Wiskott-Aldrich syndrome: diagnosis, current management, and emerging treatments | Q33415221 | ||
| Autoimmunity and infection in common variable immunodeficiency (CVID). | Q33433750 | ||
| The many faces of common variable immunodeficiency | Q33790739 | ||
| Cutaneous manifestations of DOCK8 deficiency syndrome | Q33921708 | ||
| Hyperimmunoglobulin E syndrome and tyrosine kinase 2 deficiency | Q34008074 | ||
| Evidence-based provisional clinical classification criteria for autoinflammatory periodic fevers | Q40171678 | ||
| Transfusion-associated graft-versus-host disease in severe combined immunodeficiency | Q40358922 | ||
| Noninfectious Granulomas: A Sign of an Underlying Immunodeficiency? | Q40846363 | ||
| Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency | Q40846674 | ||
| Leukocyte adhesion deficiency-I with a novel intronic mutation presenting with pyoderma gangrenosum- like lesions | Q41331976 | ||
| Distinct Cutaneous Manifestations and Cold-Induced Leukocyte Activation Associated With PLCG2 Mutations. | Q41438040 | ||
| Pattern of pediatric dermatoses at a referral centre | Q42287610 | ||
| Primary Immunodeficiency Diseases: Need for Awareness and Advocacy in India | Q45210860 | ||
| Lymphoid differentiation of hematopoietic stem cells requires efficient Cxcr4 desensitization | Q47128179 | ||
| Early Complement Component Deficiency in a Single-Centre Cohort of Pediatric Onset Lupus | Q47965723 | ||
| STING-Associated Vasculopathy with Onset in Infancy — A New Interferonopathy | Q56923367 | ||
| Cutaneous noncaseating granulomas associated with Nijmegen breakage syndrome | Q80889299 | ||
| Sarcoid-like granulomas in common variable immunodeficiency | Q83568827 | ||
| Necrobiotic cutaneous granulomas in Nijmegen breakage syndrome | Q83990318 | ||
| Blau syndrome, the prototypic auto-inflammatory granulomatous disease | Q34060987 | ||
| From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation | Q34515848 | ||
| CXCR4 signaling in health and disease | Q34532459 | ||
| GATA2 deficiency. | Q35127953 | ||
| Haematopoietic and immune defects associated with GATA2 mutation | Q35535835 | ||
| Leaky RAG Deficiency in Adult Patients with Impaired Antibody Production against Bacterial Polysaccharide Antigens | Q35695137 | ||
| GATA2 deficiency in children and adults with severe pulmonary alveolar proteinosis and hematologic disorders | Q35743114 | ||
| Multicentric dermatofibrosarcoma protuberans in patients with adenosine deaminase-deficient severe combined immune deficiency | Q35803120 | ||
| The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency | Q35931565 | ||
| Autoimmunity in wiskott-Aldrich syndrome: an unsolved enigma | Q36101320 | ||
| WHIM syndrome: a defect in CXCR4 signaling | Q36223651 | ||
| Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015. | Q36319898 | ||
| Warts and all: human papillomavirus in primary immunodeficiencies | Q36455030 | ||
| The Extended Clinical Phenotype of 26 Patients with Chronic Mucocutaneous Candidiasis due to Gain-of-Function Mutations in STAT1 | Q36480090 | ||
| Lessons from rare maladies: leukocyte adhesion deficiency syndromes | Q36588205 | ||
| Clinical predictors of primary immunodeficiency diseases in children | Q36628771 | ||
| Omenn syndrome--review of several phenotypes of Omenn syndrome and RAG1/RAG2 mutations in Japan. | Q36639621 | ||
| WHIM syndrome: congenital immune deficiency disease | Q37168887 | ||
| Papillon-Lefèvre syndrome: a series of five cases among siblings | Q37278524 | ||
| A review of genetic disorders of hypopigmentation: lessons learned from the biology of melanocytes | Q37530977 | ||
| GATA2 deficiency: a protean disorder of hematopoiesis, lymphatics, and immunity. | Q37564756 | ||
| Clinical presentation of Griscelli syndrome type 2 and spectrum of RAB27A mutations | Q37642684 | ||
| Cutaneous granulomas in common variable immunodeficiency: case report and review of literature | Q37771975 | ||
| Eponym: Papillon-Lefevre syndrome | Q37821817 | ||
| Cutaneous granulomas in ataxia telangiectasia and other primary immunodeficiencies: reflection of inappropriate immune regulation? | Q37923703 | ||
| Leukocyte adhesion deficiencies | Q37978655 | ||
| Cutaneous manifestations of primary immunodeficiency | Q38112609 | ||
| Epidermodysplasia verruciformis | Q38197065 | ||
| Complement deficiencies in systemic lupus erythematosus | Q38210887 | ||
| Cutaneous granulomas in the setting of primary immunodeficiency: a report of four cases and review of the literature | Q38379052 | ||
| Clinical presentation of human C1q deficiency: How much of a lupus? | Q38407945 | ||
| Insights from Mendelian Interferonopathies: Comparison of CANDLE, SAVI with AGS, Monogenic Lupus. | Q38966512 | ||
| STAT mutations as program switchers: turning primary immunodeficiencies into autoimmune diseases | Q38996190 | ||
| Current Status of Dedicator of Cytokinesis-Associated Immunodeficiency: DOCK8 and DOCK2. | Q39021324 | ||
| Primary immunodeficiencies worldwide: an updated overview from the Jeffrey Modell Centers Global Network | Q40070985 | ||
| P433 | issue | 6 | |
| P304 | page(s) | 391-405 | |
| P577 | publication date | 2017-11-01 | |
| P1433 | published in | Indian Dermatology Online Journal | Q15817340 |
| P1476 | title | Approach to a Child with Primary Immunodeficiency Made Simple | |
| P478 | volume | 8 |
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