Works matching IS 02719142 AND DT 2016 AND VI 36 AND IP 4

Results: 14

Immune Complex-Mediated Glomerulonephritis in a Patient with Wiskott-Aldrich Syndrome.

Published in:

2016

By:

Shigemura, Tomonari;
Nakazawa, Yozo;
Shimojo, Hisashi;
Kobayashi, Norimoto;
Agematsu, Kazunaga

Publication type:

Letter

Presenting features and platelet anomalies in WAS: one centre's experience.

Published in:

2016

By:

Tsilifis, Christo;
Gennery, Andrew;
Cant, Andrew

Publication type:

Letter

Spondylodiscitis in a Boy with X-linked Agammaglobulinemia: an Unusual Occurrence.

Published in:

2016

By:

Bhattad, Sagar;
Vignesh, Pandiarajan;
Rawat, Amit;
Suri, Deepti;
Gupta, Anju;
Vyas, Sameer;
Singh, Surjit

Publication type:

Letter

A 'Too Negative' ANA Test Predicts Antibody Deficiency.

Published in:

2016

By:

Recher, Mike;
Berger, Christoph;
Daikeler, Thomas;
Hess, Christoph;
Heijnen, Ingmar

Publication type:

Letter

Secondary Antibody Deficiency in Glucocorticoid Therapy Clearly Differs from Primary Antibody Deficiency.

Published in:

Journal of Clinical Immunology, 2016, v. 36, n. 4, p. 406, doi. 10.1007/s10875-016-0264-7

By:

Wirsum, Clemens;
Glaser, Cornelia;
Gutenberger, Sylvia;
Keller, Baerbel;
Unger, Susanne;
Voll, Reinhard;
Vach, Werner;
Ness, Thomas;
Warnatz, Klaus

Publication type:

Article

Ligase-4 Deficiency Causes Distinctive Immune Abnormalities in Asymptomatic Individuals.

Published in:

Journal of Clinical Immunology, 2016, v. 36, n. 4, p. 341, doi. 10.1007/s10875-016-0266-5

By:

Felgentreff, Kerstin;
Baxi, Sachin;
Lee, Yu;
Dobbs, Kerry;
Henderson, Lauren;
Csomos, Krisztian;
Tsitsikov, Erdyni;
Armanios, Mary;
Walter, Jolan;
Notarangelo, Luigi

Publication type:

Article

Myelodysplastic Syndrome and Acute Lymphocytic Leukemia in Common Variable Immunodeficiency (CVID).

Published in:

2016

By:

Toh, Jennifer;
Eisenberg, Rachel;
Bakirhan, Kamila;
Verma, Amit;
Rubinstein, Arye

Publication type:

Letter

Visceral Leishmaniasis May Unmask X-linked Hyper-IgM Syndrome.

Published in:

2016

By:

Gonzalez-Granado, Luis;
Dominguez-Pinilla, Nerea;
Gallego-Bustos, Fernando;
Ruiz-Contreras, Jesús;
Allende, Luis

Publication type:

Letter

Copa Syndrome: a Novel Autosomal Dominant Immune Dysregulatory Disease.

Published in:

2016

By:

Vece, Timothy;
Watkin, Levi;
Nicholas, Sarah;
Canter, Debra;
Braun, Michael;
Guillerman, Robert;
Eldin, Karen;
Bertolet, Grant;
McKinley, Scott;
Guzman, Marietta;
Forbes, Lisa;
Chinn, Ivan;
Orange, Jordan

Publication type:

Editorial

The Evolving Landscape of Primary Immunodeficiencies.

Published in:

2016

By:

Gennery, Andrew

Publication type:

Editorial

A Clinical Approach to a Child with Hypoalbuminemia and Lymphopenia.

Published in:

2016

By:

Köstel-Bal, Ayse;
Kaymak, Suna;
Haskoloğlu, Şule;
Kuloğlu, Zarife;
Ensari, Arzu;
Doğu, Figen;
Kansu, Aydan;
İkincioğulları, Aydan

Publication type:

Letter

WHIM Syndrome Caused by Waldenström's Macroglobulinemia-Associated Mutation CXCR4.

Published in:

Journal of Clinical Immunology, 2016, v. 36, n. 4, p. 397, doi. 10.1007/s10875-016-0276-3

By:

Liu, Qian;
Pan, Catherina;
Lopez, Lizbeeth;
Gao, Jiliang;
Velez, Daniel;
Anaya-O'Brien, Sandra;
Ulrick, Jean;
Littel, Patricia;
Corns, John;
Ellenburg, Donald;
Malech, Harry;
Murphy, Philip;
McDermott, David

Publication type:

Article

Erratum to: Adenosine Deaminase Deficient Severe Combined Immunodeficiency Presenting as Atypical Haemolytic Uraemic Syndrome.

Published in:

2016

By:

Nikolajeva, Olga;
Worth, Austen;
Hague, Rosie;
Martinez-Alier, Nuria;
Smart, Joanne;
Adams, Stuart;
Davies, E.;
Gaspar, H.

Publication type:

Erratum

Novel Mutations Causing C5 Deficiency in Three North-African Families.

Published in:

Journal of Clinical Immunology, 2016, v. 36, n. 4, p. 388, doi. 10.1007/s10875-016-0275-4

By:

Colobran, Roger;
Franco-Jarava, Clara;
Martín-Nalda, Andrea;
Baena, Neus;
Gabau, Elisabeth;
Padilla, Natàlia;
de la Cruz, Xavier;
Pujol-Borrell, Ricardo;
Comas, David;
Soler-Palacín, Pere;
Hernández-González, Manuel

Publication type:

Article