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Precision Health Database


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Primary Immune Deficiency Diseases

Last data update: Mar 20, 2023. (Total: 58788 Documents since 2012)
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Records 1 - 26 (of 26 Records)

Query Trace: all[original query]>>Guidelines Related[Product Type]
Consensus on diagnosis and management of Hereditary Angioedema in the Middle East: A Delphi initiative.
Maurer Marcus et al. The World Allergy Organization journal 2023 16(1) 100729
The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity.
Baris Safa et al. The journal of allergy and clinical immunology. In practice 2022
Familial Mediterranean Fever: How to Interpret Genetic Results? How to Treat? A Quarter of a Century After the Association with the Mefv Gene.
Batu Ezgi Deniz et al. Current rheumatology reports 2022
Recommendations for uniform definitions used in newborn screening for severe combined immunodeficiency.
Blom Maartje et al. The Journal of allergy and clinical immunology 2021
Hereditary angioedema in children and adolescents - A consensus update on therapeutic strategies for German-speaking countries.
Wahn V et al. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2020 Jun
Methodological quality of clinical practice guidelines for genetic testing in children: A systematic assessment using the appraisal of guidelines for research and evaluation II instrument.
Jiao Xue-Feng et al. Medicine 2019 Dec 98(52) e18521
The International/Canadian Hereditary Angioedema Guideline.
Betschel Stephen et al. Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology 2019 1572
International consensus on the use of genetics in the management of hereditary angioedema.
Germenis Anastasios E et al. The journal of allergy and clinical immunology. In practice 2019 Oct
Diagnosis and Management of Osteopetrosis: Consensus Guidelines From the Osteopetrosis Working Group.
Wu Calvin C et al. The Journal of clinical endocrinology and metabolism 2017 102(9) 3111-3123
Local Coverage Determination (LCD): Flow Cytometry (L33661)
The U.S. Centers for Medicare & Medicaid Services
[Evidence-based treatment recommendations for familial Mediterranean fever : A joint statement by the Society for Pediatric and Adolescent Rheumatology and the German Society for Rheumatology].
Kallinich T et al. Zeitschrift fur Rheumatologie 2019 Feb 78(1) 91-101
British Society for Immunology/United Kingdom Primary Immunodeficiency Network consensus statement on managing non-infectious complications of common variable immunodeficiency disorders.
Bethune C et al. Clinical and experimental immunology 2019 Jun 196(3) 328-335
Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition, Classification and Diagnosis.
Giavina-Bianchi Pedro et al. Clinics (Sao Paulo, Brazil) 2018 73e310
Recommendations for Screening and Management of Late Effects in Patients with Severe Combined Immunodeficiency after Allogenic Hematopoietic Cell Transplantation: A Consensus Statement from the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects after Pediatric HCT.
Heimall Jennifer et al. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 2017 Aug 23(8) 1229-1240
The international WAO/EAACI guideline for the management of hereditary angioedema - the 2017 revision and update.
Maurer Marcus et al. Allergy 2018 Jan
Recommendations for Childhood Cancer Screening and Surveillance in DNA Repair Disorders.
Walsh Michael F et al. Clinical cancer research : an official journal of the American Association for Cancer Research 2017 Jun 23(11) e23-e31
EULAR recommendations for the management of familial Mediterranean fever.
Ozen Seza et al. Annals of the rheumatic diseases 2016 Apr 75(4) 644-51
Guidelines for the management and treatment of periodic fever syndromes familial Mediterranean fever.
Terreri Maria Teresa R A et al. Revista brasileira de reumatologia 56(1) 37-43
Guide and Position of the International Society of Nutrigenetics/Nutrigenomics on Personalised Nutrition: Part 1 - Fields of Precision Nutrition.
Ferguson Lynnette R et al. Journal of nutrigenetics and nutrigenomics 2016 May 9(1) 12-27
ACOG Committee Opinion No. 442: Preconception and prenatal carrier screening for genetic diseases in individuals of Eastern European Jewish descent.
ACOG Committee on Genetics. Obstet Gynecol 2009 Oct (4) 950-3
Review of Select Practice Parameters, Evidence-Based Treatment Algorithms, and International Guidelines for Hereditary Angioedema.
Jose Jaison et al. Clinical reviews in allergy & immunology 2016 Apr
Canadian hereditary angioedema guideline.
Betschel Stephen et al. Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology 2014 10(1) 50
[New recommendations for the Dutch neonatal screening programmeA report from the Health Council of the Netherlands].
Cornel M C et al. Ned Tijdschr Geneeskd 2015 159(0) A9115
Evidence-based recommendations for genetic diagnosis of familial Mediterranean fever.
Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency.
Evidence-based recommendations for the practical management of Familial Mediterranean Fever.
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