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DOIs for this ISSN

Showing the top 5 of 886 DOIs, ordered by correction priority.

#	Title	Missing	Priority	Citations
1	Immunomodulation in the Treatment of Disseminated Coccidioid… (10.70962/cis2025abstract.132)	References ORCID	34.95	4
2	Thymoma-Associated Autoimmunity Is Th1 Driven and Can Be Ame… (10.70962/cis2025abstract.113)	References ORCID	15.05	1
3	Pediatric Pyoderma Gangrenosum in Patients with a Novel Bial… (10.70962/cis2025abstract.124)	References ORCID	15.05	1
4	Evaluation of Presenting Symptoms in Pediatric Patients with… (10.70962/cis2025abstract.172)	References ORCID	15.05	1
5	A Novel Dominant Negative Variant in IL2RG Gene that Failed… (10.70962/cis2025abstract.177)	References ORCID	15.05	1
6	Expanding the Allelic Spectrum of TCN2: A Case Report on Tra… (10.70962/cis2025abstract.18)	References ORCID	15.05	1
7	Unconditioned Hematopoietic Stem Cell Transplant in Hypomorp… (10.70962/cis2025abstract.184)	References ORCID	15.05	1
8	Diversity in the United States Immunodeficiency Network (USI… (10.70962/cis2025abstract.185)	References ORCID	15.05	1
9	Primary Intestinal Lymphangiectasia as a Cause of Combined I… (10.70962/cis2025abstract.19)	References ORCID	15.05	1
10	Vitamin D Deficiency Is Prevalent and Resistant to Correctio… (10.70962/cis2025abstract.195)	References ORCID	15.05	1
11	Papillon-Lefèvre Syndrome Presenting with Early-Onset Psoria… (10.70962/cis2025abstract.22)	References ORCID	15.05	1
12	WHIM Syndrome Diagnosis in a Parent and Child (10.70962/cis2025abstract.242)	References ORCID	15.05	1
13	Mavorixafor Inhibits Pathogenic Cxcr4 Signaling and Function… (10.70962/cis2025abstract.32)	References ORCID	15.05	1
14	A Cdc42 C-terminal Mutation Associated with Life-Threatening… (10.70962/cis2025abstract.42)	References ORCID	15.05	1
15	Biallelic DUOX2 Variants and the Link to Very Early-Onset IB… (10.70962/cis2025abstract.49)	References ORCID	15.05	1
16	Clinical Response Among Participants with Warts in the Phase… (10.70962/cis2025abstract.59)	References ORCID	15.05	1
17	Addition of Thiotepa to Alemtuzumab, Fludarabine, and Melpha… (10.70962/cis2025abstract.61)	References ORCID	15.05	1
18	Evaluating the Role of Genetic Testing for Inborn Errors of… (10.70962/cis2025abstract.89)	References ORCID	15.05	1
19	Validation of an Interferon Type I Score Test on the Nanostr… (10.70962/cis2025abstract.98)	References ORCID	15.05	1
20	Patient with Common Variable Immunodeficiency Type 2 Due to… (10.70962/lasid2025abstract.1)	References ORCID	15.05	1
21	Genetic Mutations, Clinical Features, and Mortality in Sever… (10.70962/arapid2025abstract.1)	References ORCID	0.00	0
22	Bone Marrow Transplantation in Severe Combined Immunodeficie… (10.70962/arapid2025abstract.10)	References ORCID	0.00	0
23	Noninfectious Manifestations in Common Variable Immunodefici… (10.70962/arapid2025abstract.11)	References ORCID	0.00	0
24	Outcomes of Hematopoietic Stem Cell Transplantation in Patie… (10.70962/arapid2025abstract.12)	References ORCID	0.00	0
25	Predictors of Mortality and Recurrence in Hemophagocytic Lym… (10.70962/arapid2025abstract.13)	References ORCID	0.00	0
26	Primary Immunodeficiency and Cancer (10.70962/arapid2025abstract.14)	References ORCID	0.00	0
27	The Enigma of Hyper-IgE Syndromes: Is There a Link Between t… (10.70962/arapid2025abstract.15)	References ORCID	0.00	0
28	Evans Syndrome in Children: A Warning Sign of an Inborn Erro… (10.70962/arapid2025abstract.16)	References ORCID	0.00	0
29	Quality of Life After Hematopoietic Stem Cell Transplantatio… (10.70962/arapid2025abstract.17)	References ORCID	0.00	0
30	Evaluation of Healthcare Personnel’s Knowledge on the Signs… (10.70962/arapid2025abstract.18)	References ORCID	0.00	0
31	Evaluation of Patients’ and Parents’ Knowledge of Inborn Err… (10.70962/arapid2025abstract.19)	References ORCID	0.00	0
32	Quality of Life in Patients with Immune Deficiency Receiving… (10.70962/arapid2025abstract.20)	References ORCID	0.00	0
33	ICF4 Syndrome: From Genetic Diagnosis to Therapeutic Approac… (10.70962/arapid2025abstract.21)	References ORCID	0.00	0
34	Successful Hematopoietic Stem Cell Transplantation in Two Ca… (10.70962/arapid2025abstract.22)	References ORCID	0.00	0
35	Vici Syndrome: A Rare Case of Combined Immunodeficiency (10.70962/arapid2025abstract.23)	References ORCID	0.00	0
36	NFKB1 Mutation and Burkitt Lymphoma: At the Crossroads Betwe… (10.70962/arapid2025abstract.24)	References ORCID	0.00	0
37	Defects in Innate and Intrinsic Immunity in Morocco: Genetic… (10.70962/arapid2025abstract.25)	References ORCID	0.00	0
38	ZNF341-Related Autosomal Recessive Hyper-IgE Syndrome: A Cas… (10.70962/arapid2025abstract.26)	References ORCID	0.00	0
39	Exploration of the Clinical and Immunogenetic Profile of Pat… (10.70962/arapid2025abstract.27)	References ORCID	0.00	0
40	Complement Deficiencies in Morocco: 6 Confirmed Cases and Va… (10.70962/arapid2025abstract.28)	References ORCID	0.00	0
41	Poikiloderma with Neutropenia: About Seven Cases (10.70962/arapid2025abstract.29)	References ORCID	0.00	0
42	Inborn Errors of Immunity-Associated Inflammatory Bowel Dise… (10.70962/arapid2025abstract.3)	References ORCID	0.00	0
43	Diagnostic of Chronic Granulomatous Disease: Experience of I… (10.70962/arapid2025abstract.30)	References ORCID	0.00	0
44	Allogeneic Hematopoietic Stem Cell Transplantation for Prima… (10.70962/arapid2025abstract.31)	References ORCID	0.00	0
45	Dermatomyositis: A Single Entity, Mosaic Phenotypes (10.70962/arapid2025abstract.32)	References ORCID	0.00	0
46	Multifocal Tuberculosis in the Immunocompromised: About 30 C… (10.70962/arapid2025abstract.33)	References ORCID	0.00	0
47	Variation of HLA-DR Expression in Patients with HLA Class II… (10.70962/arapid2025abstract.34)	References ORCID	0.00	0
48	Lymphocytophagy Is a Serious Complication of Severe Combined… (10.70962/arapid2025abstract.35)	References ORCID	0.00	0
49	Emerging Trends and Research Hotspots in Inborn Error of Imm… (10.70962/arapid2025abstract.36)	References ORCID	0.00	0
50	Clinical, Immunological, Genetic Characteristic, and Outcome… (10.70962/arapid2025abstract.4)	References ORCID	0.00	0