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                             22 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Altered Peripheral Blood Leucocyte Phenotype and Responses in Healthy Individuals with Homozygous Deletion of FHR1 and FHR3 Genes Bhasym, Angika
2019
39 3 p. 336-345
artikel
2 A Novel CARMIL2 Mutation Resulting in Combined Immunodeficiency Manifesting with Dermatitis, Fungal, and Viral Skin Infections As Well as Selective Antibody Deficiency Atschekzei, Faranaz
2019
39 3 p. 274-276
artikel
3 A Report of Novel STIM1 Deficiency and 6-Year Follow-Up of Two Previous Cases Associated with Mild Immunological Phenotype Rice, Laura
2019
39 3 p. 249-256
artikel
4 Autoinflammation with Infantile Enterocolitis Associated with Recurrent Perianal Abscesses Siahanidou, Tania
2019
39 3 p. 237-240
artikel
5 CAPS and NLRP3 Booshehri, Laela M.
2019
39 3 p. 277-286
artikel
6 Clinical Features and HSCT Outcome for SCID in Turkey Ikinciogullari, Aydan
2019
39 3 p. 316-323
artikel
7 Different Clonal T-Large Granular Lymphocyte Proliferations in SCID Savaşan, Süreyya
2019
39 3 p. 245-248
artikel
8 EBV-Related Hodgkin Lymphoma in an ICF2 Patient: Is EBV Susceptibility a Hallmark of This ICF Subtype? Licciardi, Francesco
2019
39 3 p. 234-236
artikel
9 Fatal Enteroviral Encephalitis in a Patient with Common Variable Immunodeficiency Harbouring a Novel Mutation in NFKB2 Slade, Charlotte A.

39 3 p. 324-335
artikel
10 Fatal Enteroviral Encephalitis in a Patient with Common Variable Immunodeficiency Harbouring a Novel Mutation in NFKB2 Slade, Charlotte A.
2019
39 3 p. 324-335
artikel
11 Granule Cell Neuronopathy in a Patient with Common Variable Immunodeficiency McLean-Tooke, Andrew
2019
39 3 p. 267-269
artikel
12 Hemorrhagic Pneumonia as the First Manifestation of Anhidrotic Ectodermal Dysplasia with Immunodeficiency Ichimiya, Yuko
2019
39 3 p. 264-266
artikel
13 Human DOCK2 Deficiency: Report of a Novel Mutation and Evidence for Neutrophil Dysfunction Moens, Leen
2019
39 3 p. 298-308
artikel
14 Human DOCK2 Deficiency: Report of a Novel Mutation and Evidence for Neutrophil Dysfunction Moens, Leen

39 3 p. 298-308
artikel
15 Interferon-γ Receptor 1 Deficiency Corrected by Umbilical Cord Blood Transplantation Michniacki, Thomas F.
2019
39 3 p. 257-260
artikel
16 Interleukin-36 Receptor Antagonist Deficiency (DITRA) with a Novel IL36RN Homozygous Mutation c.200G > T (P.Cys67Phe) in a Young Colombian Woman Zea-Vera, Andres F.
2019
39 3 p. 261-263
artikel
17 Molecular, Immunological, and Clinical Features of 16 Iranian Patients with Mendelian Susceptibility to Mycobacterial Disease Sarrafzadeh, Shokouh Azam
2019
39 3 p. 287-297
artikel
18 Report of a Chinese Cohort with Leukocyte Adhesion Deficiency-I and Four Novel Mutations Sun, Bijun
2019
39 3 p. 309-315
artikel
19 Revisiting Fatal Granulomatous Disease of Childhood Through an Autopsy: Still Lethal in the Developing World! Pilania, Rakesh Kumar
2019
39 3 p. 241-244
artikel
20 RNAseq Supports the Molecular Genetic Diagnosis of Late-Onset ADA Deficiency Watson, Christopher M.
2019
39 3 p. 270-273
artikel
21 Successful Rituximab Treatment for Lymphoma, Secondary Immunodeficiency Causing Debilitating Sinusitis: Underlying Primary Immunodeficiency Disease, and Alternative Treatments to Improve the Quality of Life? Bonagura, Vincent R.
2019
39 3 p. 229-230
artikel
22 Successful Treatment of Sinusitis with Topical Human Milk in a Lymphoma Patient Using Rituximab Yamaguchi, Nise
2019
39 3 p. 231-233
artikel
                             22 gevonden resultaten
 
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