Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States. - Wikidata - wikimedia - TriplyDB

Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States.

Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States.

http://www.wikidata.org/entity/Q35820252

about

Recent advances in treatment of severe primary immunodeficiencies Eosinophilia Associated with Disorders of Immune Deficiency or Immune Dysregulation Adenosine Deaminase Deficiency - More Than Just an Immunodeficiency Application of Flow Cytometry in the Evaluation of Primary Immunodeficiencies Flow Cytometry, a Versatile Tool for Diagnosis and Monitoring of Primary Immunodeficiencies Human RAG mutations: biochemistry and clinical implications Multisystem Anomalies in Severe Combined Immunodeficiency with Mutant BCL11B Adoptive immunotherapy for primary immunodeficiency disorders with virus-specific T lymphocytes Estimating the Size of the U.S. Population at Risk of Severe Adverse Events from Replicating Smallpox Vaccine.Primary Immunodeficiency Disorders in India-A Situational Review Advances in the Care of Primary Immunodeficiencies (PIDs): from Birth to Adulthood.Primary immune deficiencies - principles of care.Nijmegen breakage syndrome detected by newborn screening for T cell receptor excision circles (TRECs)What has happened in the last 50 years in immunology.Successful newborn screening for SCID in the Navajo Nation.TREC Based Newborn Screening for Severe Combined Immunodeficiency Disease: A Systematic Review History and current status of newborn screening for severe combined immunodeficiency.MALDI-TOF-MS Assay to Detect the Hemizygous 22q11.2 Deletion in DNA from Dried Blood Spots.Positive Family History, Infection, Low Absolute Lymphocyte Count (ALC), and Absent Thymic Shadow: Diagnostic Clues for All Molecular Forms of Severe Combined Immunodeficiency (SCID).IL2RG reversion event in a common lymphoid progenitor leads to delayed diagnosis and milder phenotype.Toll-like receptor signaling in primary immune deficiencies.Radiation-sensitive severe combined immunodeficiency: The arguments for and against conditioning before hematopoietic cell transplantation--what to do?Late Onset Hypomorphic RAG2 Deficiency Presentation with Fatal Vaccine-Strain VZV Infection.New insights into the metabolic and nutritional determinants of severe combined immunodeficiency.Prevalence and morbidity of primary immunodeficiency diseases, United States 2001-2007.Cost-Effectiveness/Cost-Benefit Analysis of Newborn Screening for Severe Combined Immune Deficiency in Washington State Combined immunodeficiency in the United States and Kuwait: Comparison of patients' characteristics and molecular diagnosis.Abnormal TREC-Based Newborn Screening Test in a Premature Neonate with Massive Perivillous Fibrin Deposition of the Placenta A Case of IL-7R Deficiency Caused by a Novel Synonymous Mutation and Implications for Mutation Screening in SCID Diagnosis.Newborn Screening for Severe Primary Immunodeficiency Diseases in Sweden-a 2-Year Pilot TREC and KREC Screening Study Unrelated Hematopoietic Cell Transplantation in a Patient with Combined Immunodeficiency with Granulomatous Disease and Autoimmunity Secondary to RAG Deficiency.Newborn screening for SCID: where are we now?Primary immunodeficiencies: a decade of shifting paradigms, the current status and the emergence of cutting-edge therapies and diagnostics.Severe combined immunodeficiency: recent developments and guidance on clinical management.Congenital defects in V(D)J recombination.Novel Genome-Editing Tools to Model and Correct Primary Immunodeficiencies.Severe combined immunodeficiency--an update.Newborn screening for severe combined immunodeficiency: Evaluation of a commercial T-cell receptor excision circle-based method in Victorian dried blood spots.Potential Uses and Inherent Challenges of Using Genome-Scale Sequencing to Augment Current Newborn Screening.Overview of Immunodeficiency Disorders.

P2860

Q26766170-A4A529B4-93F4-4D21-B50C-CD9838C1130D Q26799603-6ADB290E-52F1-4D61-82D2-59D13108F6BA Q26865373-142546EA-95BC-48B0-AD8C-B1DA999D26D8 Q28075586-66CBF60E-72F7-4AE6-B3BA-149F173B983A Q28076919-63AC416B-8866-4EC8-9370-4283392C3F14 Q28274274-930F8A9B-EC30-4FD7-9960-73CEBF4C9AC3 Q29147572-5ADEDA7E-6F74-4FBB-8085-EACCD9585D09 Q29393780-BF34D868-1AB3-489C-BE5C-45C80F8CD612 Q30151714-D5AE4AD3-C8A1-494C-9E09-D1B54CE7E53C Q33809534-A3D8E84A-EE8B-41FB-AE16-487C9FB2A165 Q33849434-8A90D24D-DB64-4509-A934-771DB94363FA Q34700023-52490726-9A03-4825-AC5B-85CD7977F716 Q35155231-73CC8C5D-9D29-4936-9D96-3A1CD76BE5E5 Q35560218-070BF6CB-8D61-4522-9396-ADDA1FDF16C3 Q35572104-7EA31D98-9300-445B-9149-502C1FC0CC25 Q35609753-3C2AAC13-30BE-470E-970F-148474EFC7D6 Q35613205-FC828D54-EF7E-4733-9A0A-E544D3ADD789 Q35846619-3F7DD362-C9CE-470B-B6CB-E21F54F1C722 Q35846963-8243A0B6-A1F1-4989-AF05-09EA13A63BA4 Q35858596-7FDFC100-9104-4E43-A2BF-8E9A7705E08A Q36238886-E14E7803-C35F-49EA-8D60-8CC3C34CEDA6 Q36269199-6AFAD46F-AE5A-4B5B-8093-E087CB40456B Q36326820-5A89801F-9BCB-4FB3-BFD1-8CFF718AC225 Q36756917-C3EED5A2-DEB6-405D-9802-C9419ED8BECC Q36763235-EFDEE20C-A739-4534-92A1-91ABBCED91C2 Q36839938-ACBA9A6B-AB17-46AB-B907-74A2C5417D3A Q36908611-9BA059E6-7805-47AD-A88B-F50F268CF0EC Q37043805-D3768C39-A1EB-45A9-B49C-2A2C04ABA7D2 Q37368919-16D7A1B6-6C07-4746-9EFB-EF99298559FA Q37580857-D33AB34E-888D-4877-89B7-7DCA9D554D9B Q37618790-565899B5-6107-459D-A6D4-11B76E5B70AE Q38267187-3D8526CA-809F-49AA-9192-68BCF00EE9BE Q38289442-27167017-481B-404E-9368-89E6DB19BF5B Q38309572-68ED680E-928C-4152-B857-EF7FD4C643CF Q38490471-DEB924A5-6207-4A1B-BDFA-E788B8639CAE Q38519892-88CDA97D-1A6A-44A2-8155-819F19A9B2E7 Q38559463-99E74E85-EF9F-498B-B565-F06C40D25A1F Q38598306-65597AAC-D993-4543-A1DA-3FE3E8EF5D76 Q38599808-56CE1762-0783-46BF-AA6C-1AAE69DB709F Q38603706-657AFA22-3096-4FDC-9C2C-9D625D9464B0

P2860

Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States.

http://www.wikidata.org/entity/Q35820252

description

2014 nî lūn-bûn

@nan

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

2014年论文

@zh

2014年论文

@zh-cn

name

Newborn screening for severe c ...... programs in the United States.

@ast

Newborn screening for severe c ...... programs in the United States.

@en

type

label

Newborn screening for severe c ...... programs in the United States.

@ast

Newborn screening for severe c ...... programs in the United States.

@en

prefLabel

Newborn screening for severe c ...... programs in the United States.

@ast

Newborn screening for severe c ...... programs in the United States.

@en

P1433

Q35820252-EE989B9A-0CF4-4120-9231-97CAA5DEC025

P1476

Q35820252-8B8A0B5B-9867-45AF-9249-8B83B2CD27D7

P2093

Q35820252-016B69FC-00CD-4DF0-A75D-C74A462514EF

Q35820252-0621099F-DB4F-422F-A0B5-B21991D9ECDD

Q35820252-06B3466D-F269-409B-9C23-C8E55683AEDB

Q35820252-08765E69-FAC5-4F2B-9C0F-D32405A14FD9

Q35820252-0914001C-5487-4E2C-8ED1-1C1E236B1476

Q35820252-10617B9A-E18E-4BED-A07A-C7AC30948CA3

Q35820252-11EC10AC-D744-46E5-92E6-A7F19B32D9B1

Q35820252-13166E10-4DE6-4795-9E7B-6DB887C275C3

Q35820252-13E1903E-6D85-4245-BF80-E94E70803951

Q35820252-190B96FA-4E8D-448B-9787-ADC7BFAFB48B

P2860

Q35820252-115F21DD-33F5-4CDD-945D-8D58543B531E

Q35820252-1642A9CD-FB79-4B82-98B2-9A60F6B7A1FF

Q35820252-196439F4-7A3F-4BCB-A1C0-9623B0EAD8DE

Q35820252-1CC501CC-A52D-47B6-B50D-EBE3C7C2B620

Q35820252-263B3443-2005-40C5-9FD2-8EE754CC952D

Q35820252-2C73553A-A442-49B9-B069-5D01DC6BB32D

Q35820252-2CDB7363-11C9-4C1F-934F-C08E3D86230E

Q35820252-2D853AEF-1E9B-40F8-B1B7-31E8234C7E28

Q35820252-35CF7309-9A99-4CD1-84B2-19F36291FD14

Q35820252-3DD4C94E-30D2-42BB-BC64-D8E961B3A86A

P304

Q35820252-E3560E9D-3E30-41AB-8F97-FF308CF4C92A

P31

Q35820252-8D51C256-7448-4F8C-A2FD-993FFDB83D5F

P356

Q35820252-4FCF5A35-DD7B-48C0-B409-296CC0763F05

P407

Q35820252-882C1A06-7E52-49DF-A1A5-99968E99152E

P433

Q35820252-E0C403D8-E836-4906-9834-5F119A1EBDD8

P478

Q35820252-489A0E0E-F6C5-48F9-A0D7-817BD1EB7EDC

P50

Q35820252-0F7E1044-9CB7-41F8-A15D-8C179665221A

Q35820252-10EC50F6-BDB0-414E-8234-EBFB81F14820

Q35820252-1FB6182F-4D02-42EB-9E43-DB1AE1AC02A2

Q35820252-4C3B63E5-A43B-40AF-9EDC-57C79AF22316

Q35820252-50D606FB-0048-42CA-8EC6-E55565981413

Q35820252-59AAEBFB-2150-47DD-B0C3-B7C4011A2F28

Q35820252-CB221175-BFA7-4B36-8A29-FCCABAF4C1B0

Q35820252-E098F6A9-A989-4161-B401-4E6ADEEDB599

P577

Q35820252-5F3F6059-36BF-4F38-8C20-F176BFC2D350

P5875

Q35820252-5EF26957-F4C2-486C-916E-F4EFAD7BEE84

P698

Q35820252-39DF9AD1-DD51-4E98-8243-CA477DFA8DE4

P932

Q35820252-664B0A1D-5275-4C82-81BA-1C1E04AD4F50

P356

P1433

Journal of the American Medical Association

P1476

Newborn screening for severe c ...... programs in the United States.

@en

P2093

Adrienne Manning

http://www.w3.org/2001/XMLSchema#string

Aly Abdel-Mageed

http://www.w3.org/2001/XMLSchema#string

Amy Brower

http://www.w3.org/2001/XMLSchema#string

Anne B Yates

http://www.w3.org/2001/XMLSchema#string

Anne Marie Comeau

http://www.w3.org/2001/XMLSchema#string

Anthony Infante

http://www.w3.org/2001/XMLSchema#string

Antonia Kwan

http://www.w3.org/2001/XMLSchema#string

Arye Rubenstein

http://www.w3.org/2001/XMLSchema#string

Beth Vogel

http://www.w3.org/2001/XMLSchema#string

Beverly N Hay

http://www.w3.org/2001/XMLSchema#string

P2860

Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency

Newborn screening for SCID identifies patients with ataxia telangiectasia

Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution

Development of population-based newborn screening for severe combined immunodeficiency

Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia

Newborn Screening for Severe Combined Immunodeficiency; The Wisconsin Experience (2008–2011)

Recommendations for live viral and bacterial vaccines in immunodeficient patients and their close contacts.

Newborn screening for SCID in New York State: experience from the first two years.

A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans.

Transplantation outcomes for severe combined immunodeficiency, 2000-2009.

P304

729-738

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1001/JAMA.2014.9132

http://www.w3.org/2001/XMLSchema#string

P407

P433

7

http://www.w3.org/2001/XMLSchema#string

P478

312

http://www.w3.org/2001/XMLSchema#string

P50

William T. Shearer

Charlotte Cunningham-Rundles

Vincent R Bonagura

Erwin W. Gelfand

P577

2014-08-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

265294433

http://www.w3.org/2001/XMLSchema#string

P698

25138334

http://www.w3.org/2001/XMLSchema#string

P932

4492158

http://www.w3.org/2001/XMLSchema#string