ABDELKADER S. INTERLUKIN 12 RECEPTOR BETA 1 (IL12RB1) DEFICIENCY

AL ALWI Z. MATCHED UNRELATED DONOR HEMATOPOIETIC STEM CELL TRANSPLANTATION, EFFECTIVELY RESOLVED THE CLINICAL AND IMMUNOLOGICAL DEFECTS IN A PATIENT WITH INTERLEUKIN-2-RECEPTOR ALPHA DEFICIENCY

ALEMAYEHU TEKLE T. RECURRENT INFECTIONS IN AN ETHIOPIAN INFANT WITH A CONGENITAL T-CELL IMMUNODEFICIENCY – DIGEORGE SYNDROME

AL-HERZ W. CHARACTERISTICS OF VIRAL INFECTIONS AMONG PRIMARY IMMUNODEFICIENT CHILDREN

ALJOHANI A. VARIABLE CLINICAL PHENOTYPE OF PATIENTS WITH TFRC GENE MUTATION

ALSHEHRI S. PATIENT WITH HOMOZYGOUS LOSS-OF-FUNCTION STAT-1 MUTATION UNDERWENT HAPLOIDENTICL STEM CELL TRANSPLANT: CASE REPORT

ANDREJEVIC S. HEREDITARY ANGIOEDEMA WITH C1 INHIBITOR DEFICIENCY AND SYSTEMIC AUTOIMMUNE DISEASES: A  SINGLE CENTRE SERBIAN STUDY ON EIGHTY-TWO PATIENTS

ASGARDOON M.H. THE INHIBITORY ROLE OF M2000 (B-D-MANNURONIC ACID) ON EXPRESSION OF TOLL-LIKE RECEPTOR 2 AND 4 IN HT29 CELL LINE

ATSCHEKZEI F. A NOVEL CARMIL2 MUTATION RESULTING IN COMBINED IMMUNODEFICIENCY MANIFESTING WITH DERMATITIS, FUNGAL AND VIRAL SKIN INFECTIONS AS WELL AS SELECTIVE ANTIBODY DEFICIENCY

AYTEKIN C. A RARE AUTOSOMAL RECESSIVE AGAMMAGLOBULINEMIA: IGLL1 (LAMBDA 5)  GENE MUTATION

AZIZI G. THERAPEUTIC APPROACH BY SIROLIMUS FOR ENTEROPATHY TREATMENT IN LRBA DEFICIENCY

AZIZI G. APPROACH TO THE DIAGNOSIS OF AUTOIMMUNITY IN PRIMARY IMMUNODEFICIENCY

BAGHERI Y. COMPARISON OF CLINICAL AND IMMUNOLOGICAL FEATURES AND MORTALITY IN COMMON VARIABLE IMMUNODEFICIENCY AND AGAMMAGLOBULINEMIA PATIENTS FOR PATIENTS MANAGEMENT

BAKHSHESH S. SELECTIVE IMMUNOGLOBULIN M DEFICIENCY: IS IT TRULY AS RARE AS REPORTED?

BANDAY A. SEVERE ATOPIC DERMATITIS AS THE PRESENTING MANIFESTATION OF A CHILD WITH SEVERE COMBINED IMMUNODEFICIENCY.

BANDAY A. EXOME SEQUENCING FOR DIAGNOSIS OF AN UNUSUAL CAUSE OF NEUTROPENIA.

BANSIE R. A PHASED PROGRAM FOR THE INITIATION OF SCREENING FOR PRIMARY IMMUNE DEFICIENCIES IN SURINAME

BARASA A. PRIMARY IMMUNODEFICIENCY IN A LOW RESOURCE SETTING – A REPORT OF TWO CASES

BASELLI L.A. TRANSIENT VERSUS PERSISTENT HYPOGAMMAGLOBULINEMIA: CAN WE PREDICT THE OUTCOME?

BATANEANT M. CLINICAL AND IMMUNOLOGICAL EVOLUTION IN WHIM SYNDROME

BATTIATO S. RARE PARENTS: AN EXPERIENTIAL AND INFORMATIVE GROUP ABOUT  WELL-BEING IN PRIMITIVE IMMUNODEFICIENCIES

BELOIA A. THE CLINICAL AND SOCIO-ECONOMICAL IMPACT OF IMMUNOGLOBULIN CRISIS – A SINGLE ROMANIAN CENTER REPORT

BERNATOWSKA E. J PROJECT TO DISCOVER SIMILARITY AND DIFFERENCES BETWEEN THE PATIENTS WITH THE PRIMARY IMMUNODEFICIENCY IN EASTER – CENTRAL EUROPE AND IN OTHER COUNTRIES

BLAS-ESPADA J. PHENOTYPIC HETEROGENEITY IN THREE PATIENTS WITH NF-<KAPPA>B1 DEFICIENCY

BONDARENKO A. MUCOSA-ASSOCIATED LYMPHOID TISSUE 1 (MALT1) DEFICIENCY: SEVERE SKIN LESIONS AS AN EARLY DIAGNOSTIC CLUE 

BOYARCHUK O. IMPLEMENTATION OF THE MODEL OF COMBINING PHYSICIAN EDUCATION AND PUBLIC AWARENESS WITH THE INFRASTRUCTURE TO DIAGNOSE PRIMARY IMMUNODEFICIENCY DISEASES IN CHILDREN

BUI C.B. NOVEL ELANE GENE MUTATION IN A VIETNAMESE BOY WITH SEVERE CONGENITAL NEUTROPENIA

BURBELA E. MARSHALL SYNDROME AS A MULTIDISCIPLINARY PROBLEM OF CHILDHOOD

CABRERA-MARANTE O. SPEEDY DIAGNOSIS OF ANTIBODY DEFICIENCIES WITH THE MEASUREMENT OF SERUM-FREE LIGHT CHAINS

CAGDAS AYVAZ D.N. CLINICAL AND LABORATORY FEATURES OF PATIENTS WITH HYPERIMMUNOGLOBULIN M SYNDROME

CAGDAS AYVAZ D.N. SEVERE CMV RETINITIS IN AN ADULT PATIENT WITH CARMIL2 (RLTPR) DEFICIENCY

CAMONAYAN-FLOR K.A. IMMUNODEFICIENCY IN A CHILD PRESENTING WITH ECTHYMA GANGRENOSUM AND NORMAL IMMUNOGLOBULIN LEVELS

CAMPBELL M. INVESTIGATING THE LONG-TERM OUTCOMES OF ADULT PATIENTS WHO UNDERWENT HAEMATOPOIETIC STEM CELL TRANSPLANT FOR PRIMARY IMMUNODEFICIENCY DURING CHILDHOOD

CARRABBA M. CVID : ARE GENETICS AND PHENOTYPES RELATED?

CASAMAYOR-POLO L. DIAGNOSTIC ALGORITHM FOR AUTOIMMUNE LYMPHOPROLIFERATIVE SÍNDROME

CHENG K. A LITERATURE REVIEW ON SHARED DECISION-MAKING TO INFORM THE DEVELOPMENT OF AN SDM TOOL IN PRIMARY IMMUNODEFICIENCY DISEASES

CHIRIACO M. NOVEL SAMD9 GENE MUTATION IN A PATIENT WITH SKELETAL SYSTEM COMPLICATION AFTER HSCT: A CASE OF MIRAGE SYNDROME?

CLODI E. CLINICAL EFFICACY, SAFETY AND TOLERABILITY OF A 16.5% SUBCUTANEOUS IMMUNOGLOBULIN (SCIG) PREPARATION IN PEDIATRIC PRIMARY IMMUNE DEFICIENCY (PID) PATIENTS

CORNELISSEN H.M. SPUR TB TO? WHAT IS ON THE MENU?

DE FELIPE B. SCREENING FOR SEVERE T AND B CELL LYMPHOPENIAS IN ANDALUCIA USING 3 TECHNIQUES

DE WIT J. SKIN DISORDERS ARE PROMINENT FEATURES IN CAUCASIAN PATIENTS WITH PRIMARY IMMUNODEFICIENCY DISEASES: A QUESTIONNAIRE-BASED STUDY IN PEDIATRIC AND ADULT PATIENTS

DEL PINO MOLINA L. EXPLORING NEW MECHANISMS TO UNDERSTAND THE COMPLEX B CELL DYSREGULATION PRESENT IN COMMON VARIABLE IMMUNODEFICIENCY: IMPAIRED CPG DEMETHYLATION ASSOCIATES WITH B CELL PHENOTYPE AND PROLIFERATION RATE. 

DELAVARI F. DOCK8 MUTATION, A CASE REPORT ON APPLICATION OF GENETICS IN MEDICINE

DI NATALE M. NK CELLS AS A NEW BIOMARKER OF POTENTIAL RISK OF DEVELOPING CLINICAL COMPLICATIONS IN PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY.

DI NATALE M. NEW THERAPEUTIC OPTION WITH MUCOSAL AUTOVACCINE IN PATIENTS WITH SUPPURATIVE HIDRADENITIS.

DROBYSHEVSKAIA V. QUANTITATIVE DETERMINATION OF TREK AND KREC DNA MOLECULES IN THE UMBILICAL BLOOD OF THE NEWBORNES OF SAINT PETERSBURG.

EL KETTANI A. GENERALIZED VERRUCOSIS AND HPV SUSCEPTIBILITY ASSOCIATED WITH COMBINED IMMUNE DEFICIENCY

ELMAS B. DEVELOPMENT OF HODGKIN LYMPHOMA IN A PATIENT WITH COMMON VARIABLE IMMUNODEFICIENCY

EL-OWAIDY R. PERFORMANCE OF HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS FEATURES AMONG CHILDREN WITH SEVERE SEPSIS

ERRAMI A. NONSENSE MUTATION OF IL12RB1 GENE IN THREE MOROCCAN CHILDREN WITH SEVERE MYCOBACTERIAL INFECTIONS

ESTEVE-SOLE A. ALTERATIONS IN THE IL-12/IFN-GAMMA AXIS AS A MECHANISM OF SUSCEPTIBILITY TO INTRAMACROPHAGIC INFECTIONS

EURELINGS L. LYMFOPENIA AS A PREDICTOR OF SARCOIDOSIS IN PATIENTS WITH A FIRST EPISODE OF UVEITIS

FABBRIZZI F.  SAFETY AND TOLERABILITY DATA ON KEDRION 5% IVIG – A PHARMACOVIGILANCE DATABASE ANALYSIS

FADIL I. CLINICAL AND BIOLOGICAL FEATURES OF 26 MOROCCAN PATIENTS WITH HYER-IGE SYNDROME

GARCIA GARCIA A. FIRST-TIME REPORTED NECROTIZING PNEUMONIA BY TYROMICES FISSILIS IN CHRONIC GRANULOMATOUS DISEASE

GENEL F. THE EFFECT OF HOME-BASED TREATMENT WITH IMMUNOGLOBULIN ON PSYCHIATRIC ASPECTS IN PATIENTS WITH PRIMARY IMMUNODEFICIENCIES

GLADIATOR A. INFUSION PARAMETERS AND KEY CHARACTERISTICS BY AGE GROUP OF PATIENTS WITH PRIMARY IMMUNODEFICIENCY DISEASES INITIATED ON IG20GLY IN A PATIENT PROGRAM

GODA R. CHRONIC STAPHYLOCOCCUS AUREUS CARRIERS A POSSIBLE PRIMARY IMMUNODEFICIENCY DISEASE: A CASE REPORT.

GÓMEZ F. F. AGAMMAGLOBULINEMIA LINKED TO THE CHROMOSOME X: MULTIDISCIPLINARY APPROACH

GONZÁLEZ GRANADO I. COST ANALYSIS OF IV AND SC IMMUNOGLOBULINS USED IN THE TREATMENT OF PRIMARY IMMUNODEFICIENCY DISEASES IN SPAIN

GOUDOURIS E. SEVERE PULMONARY DISEASE IN TWO SIBLINGS WITH X LINKED AGAMMAGLOBULINEMIA: POSSIBLE CONTRIBUTION OF MUTATIONS IN TUMOR GROWTH FACTOR BETA 1 AND TUMOR NECROSIS FACTOR SIGNALING PATHWAY.

GUEVARA-HOYER K. PROACTIVE: PROPHYLAXIS OF RECURRENT RESPIRATORY TRACT INFECTIONS BY MUCOSAL IMMUNISATION IN COMMON VARIABLE IMMUNODEFICIENCY (PRELIMINARY RESULTS).

GUFFROY A. ADOLESCENTS AND YOUNG ADULTS (AYAS) WITH PIDS: ORGANIZE THE TRANSITION FROM AN ADULT DEPARTMENT PERSPECTIVE

GUGLIELMETTI S. X-LINKED CHRONIC GRANULOMATOSIS: MOLECULAR AND CELLULAR MECHANISMS UNDERLYING INTESTINAL INFLAMMATION

GUILLEN ROCHA N.L. SEVERE COMBINED IMMUNE DEFICIENCY WITH DISSEMINATED MYCOBACTERIUM TUBERCULOSIS INFECTION AFTER BCG VACCINATION

GULERIA S. EARLY ONSET INFLAMMATORY BOWEL DISEASE  IN A CHILD WITH X-LINKED INHIBITOR OF APOPTOSIS PROTEIN DEFICIENCY WITH A NOVEL MUTATION

GULERIA S. RASH IN NEONATES IS NOT ALL BENIGN

GUMMADI A. NOVEL MUTATIONS IN ADENOSINE DEAMINASE DEFICIENT SEVERE COMBINED IMMUNODEFICIENCY: OUR EXPERIENCE AT CHANDIGARH, NORTH INDIA

GUMMADI A. X-LINKED CARRIERS OF CHRONIC GRANULOMATOUS DISEASE: AN UNEXPLORED VISTA

GUPTA L. MICROSPORIDIAL MYOSITIS IN ADULT ONSET IMMUNODEFICIENCY: CASE-BASED REVIEW

GUPTA M. COMBINED IMMUNODEFICIENCY DISORDER DUE TO ZAP-70 DEFICIENCY: REPORT ON TWO CASES.

GUTIERREZ C. A VERSATILE MULTIPLEX QPCR ASSAY FOR THE SCREENING OF SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED AGAMMAGLOBULINEMIA AND SPINAL MUSCULAR ATROPHY IN NEWBORNS

HAHN S. APPLICATION OF TARGETED PROTEOMICS USING IMMUNO-SRM FOR POTENTIAL NEWBORN SCREENING OF PRIMARY IMMUNODEFICIENCY DISORDERS (PIDD)

HARIYAN T. CHILDREN’S IMMUNOLOGY: TEAMWORK

HERMANS M. CHRONIC SPONTANEOUS URTICARIA AS AUTO-IMMUNE FEATURE IN COMMON VARIABLE IMMUNODEFICIENCY

HILFANOVA A.M. LEUKOCYTE ADHESION DEFICIENCY TYPE III – THE FIRST CASES IN EASTERN EUROPE

HUSSAIN I. IMMUNE GLOBULIN SUBCUTANEOUS (HUMAN) 20% SOLUTION TOLERABILITY AND INFUSION CHARACTERISTICS IN PEDIATRIC AND ADVANCED-AGE PATIENTS WITH PRIMARY IMMUNODEFICIENCY

IJSPEERT H. ANTI-INTERFERON GAMMA AND IL-17 AUTOANTIBODIES IN A CHILD WITH ULCERATION AFTER BACILLUS CALMETTE-GUERIN (BCG) VACCINATION AND ONYCHOMYCOSIS

JAMEE M. CLINICAL AND RADIOLOGICAL FINDINGS IN IRANIAN PATIENTS WITH  CHRONIC GRANULOMATOUS DISEASE

JANDUS P. RATIONALE AND DESIGN OF A NONINTERVENTIONAL STUDY ON THE USAGE AND OUTCOMES OF CUVITRU IN PATIENTS OF ANY AGE WITH PRIMARY IMMUNODEFICIENCY DISEASES: CORE STUDY

JEDDANE L. INBORN ERRORS OF IMMUNITY : WHAT’S NEW IN LAST IUIS CLASSIFICATION ?

JOHNSON B. NEXT GENERATION SEQUENCING WITH COPY NUMBER ANALYSIS FOR PRIMARY IMMUNODEFICIENCIES: FINDINGS FROM A COHORT OF OVER 3,900 UNRELATED PATIENTS

KANE A. CUTANEOUS MANIFESTATIONS OF PRIMARY IMMUNODEFICIENCIES IN SENEGALESE CHILDREN : ABOUT 4 CASES

KARACA N. EBV NEGATIVE LYMPHOMA IN A PATIENT WITH MAGT1 DEFICIENCY

KARACA N. REFRACTORY CMV INFECTION IN SEVERE COMBINED AND COMBINED IMMUNODEFICIENCIES:  RAG1, ZAP70 AND ORAI1 GENE DEFECTS

KARAKOC AYDINER E. PATIENT’S ATTITUDES FOR ROUTE OF IMMUNOGLOBULIN REPLACEMENT THERAPY; MARMARA EXPERIENCE

KARIM A. STAT3 ACCUMULATES IN RESPONSE TO IL-6 DRIVEN EXPRESSION OF RANTES (CCL5) AND OTHER KB DEPENDENT GENES IN A PATIENT WITH AUTOSMOAL DOMINANT HYPER IGE SYNDROME.

KASAP N. PHENOTYPIC ANALYSIS OF DERMATITIS CAN DISTINGUISH HYPER IGE SYNDROME FROM ATOPIC DERMATITIS

KASAP N. CLINICAL AND LABORATORY MARKERS DIFFERENTIATE HYPER IGE SYNDROME FROM SEVERE ATOPIC DERMATITIS

KASMI Z. DIAGNOSIS OF CONGENITAL NEUTROPENIA

KAUR A. HEREDITARY ANGIOEDEMA IN CHILDREN: A CLINICAL EXPERIENCE OVER 20 YEARS FROM NORTH WEST INDIA.

KAUR A. PARTIAL DIGEORGE SYNDROME IN A CHILD WITH RECURRENT INFECTIONS

KECHOUT N. RECURRENT SALMONELLA ENTERITIDIS MENINGITIS AS ATYPICAL PRESENTATION OF MHC CLASS II DEFICIENCY

KEREN M. COMMON VARIABLE IMMUNE DEFICIENCY : TWO CASES WITH EARLY AND LATE DIAGNOSIS

KESHAVARZ-FATHI M. A CASE REPORT OF GRISCELLI SYNDROME TYPE 2; MUTATION, PROGNOSIS AND TREATMENT

KESHAVARZ-FATHI M. MANIFESTATIONS OF IMMUNODEFICIENCY IN AN IRANIAN PATIENT WITH HERMANSKY-PUDLAK SYNDROME TYPE 2, A NOVEL VARIANT IN AP3B1 GENE

KOCAMIS B. PHYSICIANS’ KNOWLEDGE AND ATTITUDES FOR IGG REPLACEMENT THERAPY FOR PRIMARY IMMUNODEFICIENCY IN TURKEY 

KP S. IDENTIFYING CHILDREN WITH PRIMARY IMMUNODEFICIENCY DISORDERS FOR DEVELOPING EFFECTIVE PREVENTION STRATEGIES : EVIDENCE FROM SOUTH INDIA

KREIL T.R. MEASLES VIRUS NEUTRALIZING ANTIBODIES IN IMMUNOGLOBULIN LOTS PRODUCED FROM PLASMA COLLECTED IN EUROPE OR THE UNITED STATES

KUMAR A. NOVEL MUTATIONS AND CLINICAL EXPERIENCE IN A SINGLE CENTRE COHORT OF PATIENTS WITH HEREDITARY ANGIOEDEMA FROM NORTH INDIA

KUMAR A. GRANULOMATOUS HEPATITIS AND HYPOGAMMAGLOBULINEMIA IN A YOUNG GIRL CAUSED BY NOVEL MUTATION IN ZBTB24 GENE

KUMRAH R. A CHILD WITH SEVERE COMBINED IMMUNODEFICIENCY AND A NOVEL COMPOUND HETEROZYGOUS VARIANTS IN JAK3

KUTUKCULER N. DEFICIENCY OF INTERLEUKIN-1 RECEPTOR ANTAGONIST; A CASE WITH LATE ONSET SEVERE INFLAMMATORY ARTHRITIS, NAIL PSORIASIS WITH ONYCHOMYCOSIS AND WELL RESPONSIVE TO ADALIMUMAB NOT TO CANAKINUMAB THERAPY

LAHMAR O. ASSOCIATION BETWEEN VITAMIN D METABOLISM GENE POLYMORPHYSMS AND RISK OF ADULT’S ASTHMA

LATYSHEVA E. EFFICACY, TOLERABILITY AND SAFETY OF CUTAQUIG®, SUBCUTANEOUS HUMAN IMMUNGLOBULIN 16.5%, IN ADULT PATIENTS WITH PRIMARY IMMUNODEFICIENCIES

LÓPEZ-NEVADO M. NEWBORN SCREENING FOR SEVERE COMBINED IMMUNODEFICIENCY BY QUANTIFICATION OF T-CELL EXCISION CIRCLES AND KAPPA DELETING RECOMBINATION EXCISION CIRCLES IN GUTHRIE CARD: FIRST PILOT STUDY IN MADRID

LUO D. POPULATION PHARMACOKINETIC ANALYSIS OF 3-WEEKLY AND 4-WEEKLY PRIVIGEN® IN JAPANESE PATIENTS WITH PRIMARY IMMUNODEFICIENCY

MACIAS ABRAHAM C.M. NATIONAL COMPREHENSIVE CARE PROGRAM FOR CUBAN PRIMARY IMMUNODEFICIENCY PATIENTS 2013-2019. 

MAHALLEH M. PERSISTENT SEVERE CONGENITAL NEUTROPENIA : A NOVEL HETEROZYGOUS VARIANT IN ELANE

MAHLAOUI N. CHRONIC RHINOSINUSITIS IN AGAMMAGLOBULINEMIA AND HYPER-IGM SYNDROME, SURVEY OF THE FRENCH POPULATION

MALBRAN E. A NEW CYTOTOXIC-T-LYMPHCYTE-ANTIGEN-4 (CTLA4) MUTATION, SEGREGATING WITH OSTOPOROSIS

MANUSAMA O. DEPRESSIVE MOOD DISORDERS IN RELATION TO T CELL ABNORMALITIES IN A COHORT OF COMMON VARIABLE IMMUNE DEFICIENCY PATIENTS

MASOUD S. KNOWLEDGE AND PRACTICE OF PRESCRIBING POLYCLONAL HUMAN IMMUNOGLOBULIN THERAPY BY THE DOCTORS IN REFERRAL TEACHING HOSPITALS IN KHARTOUM  IN 2018

MEJÍA GONZÁLEZ M.A. IDENTIFICATION OF A NOVEL MUTATION IN TICAM1 IN A PATIENT WITH HERPES SIMPLEX ENCEPHALITIS.

MESA-NÚÑEZ C. GENE THERAPY FOR LEUKOCYTE ADHESION DEFICIENCY TYPE I (LAD-I): A NEW THERAPEUTIC ALTERNATIVE FOR SEVERE PATIENTS.

MESHAAL S. LRBA AND CTLA4 DEFICIENCY AMONG CVID EGYPTIAN  PATIENTS

MIJANOVIC R. MALIGNANCY AMONG PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY: A SINGLE-CENTER EXPERIENCE

MILITO C. LOW DOSE AZITROMYCIN  PROPHYLAXIS IN PRIMARY ANTIBODY DEFICIENCIES:  A MULTICENTER, DOUBLE-BLIND, PLACEBO-CONTROLLED RANDOMIZED CLINICAL TRIAL

MISHRA V. REPORT OF PRIMARY IMMUNODEFICIENCY DISORDERS FROM A TERTIARY CARE HOSPITAL IN SUB- HIMALAYAN REGION IN NORTH WEST INDIA

MISHRA V. TITLE:LEUKOCYTE ADHESION DEFICIENCY DIAGNOSED ON THE  BASIS OF CLINICAL FEATURES AND COMPLETE HEMOGRAM FROM A RESOURCE LIMITED SETTING IN SUB-HIMALAYAN REGION OF NORTH-WEST INDIATITLE:LEUKOCYTE ADHESI

MOKHANTAR K. MOROCCAN CLASSIFICATION OF THE COMMON VARIABLE IMMUNODEFICIENCY

MOMTAZMANESH S. A NOVEL VPS13B FRAMESHIFT MUTATION IN A NEUTROPENIC PATIENT WITH COHEN SYNDROME

MUNTEANU A.N. PERIPHERAL IMMUNE CELL MARKERS IN CHILDREN WITH RECURRENT RESPIRATORY INFECTIONS IN THE ABSENCE OF PRIMARY IMMUNODEFICIENCY

MURÁNYI A. SYRINGEABILITY AND INJECTABILITY COMPARISON OF COMMERCIALLY AVAILABLE HUMAN SUBCUTANEOUS IGG DRUG PRODUCTS

NDIAYE M.T. VERRUCIFORM EPIDERMODYSPLASIA: THREE CASES REPORTS

NEHME – ÁLVAREZ D. A 4 YEARS EXPERIENCE IN PRIMARY IMMUNODEFICIENCIES DIAGNOSIS USING NEXT-GENERATION SEQUENCING IN HOSPITAL 12 OCTUBRE IN MADRID.

NUÑEZ DEL PRADO ALANES N. PRIMARY IMMUNE DEFICIENCIES IN BOLIVIA: CASE SERIES

OCHOA GRULLÓN J.L. EVALUATION OF POLYSACCHARIDE TYPHIM VI ANTIBODY RESPONSE AS A PREDICTOR OF HUMORAL IMMUNODEFICIENCY IN HAEMATOLOGICAL MALIGNANCIES

O’FARRILL P. CLINICAL CHARACTERISTICS IN ADULT PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA

O’FARRILL P. NK CELLS AND THEIR ROLE IN COMMON VARIABLE IMMUNODEFICIENCY

ORHAN M.F. IN DIFFERENTIAL DIAGNOSIS OF IDIOPATHIC THROMBOCYTOPENIC PURPURA: WISKOTT-ALDRICH SYNDROME

OSYPCHUK D. HYPER IGE SYNDROME ASSOCIATED WITH NOVEL DOCK8 HETEROZYGOUS MUTATION

PACILLO L. REFRACTORY/RELAPSED AUTOIMMUNE CYTOPENIAS AS CLINICAL MANIFESTATION OF PRIMARY IMMUNODEFICIENCY

PANDIARAJAN V. OUR EXPERIENCE WITH SEVERE COMBINED IMMUNODEFICIENCY IN NORTH INDIA

PANDIARAJAN V. CLINICAL AND MOLECULAR FEATURES OF CHRONIC GRANULOMATOUS DISEASE: A 26 YEARS’ EXPERIENCE FROM A TERTIARY-CARE CENTRE IN NORTH INDIA

PASQUET M. PID4KIDS: A THERAPEUTIC EDUCATION PROGRAM DEVOTED TO CHILDREN WITH PIDS CONDUCTED COOPERATIVELY BY IMMUNOLOGY STUDENTS AND CARE UNIT

PATRA P. AUTOIMMUNITY IN WISKOTT-ALDRICH SYNDROME; DOES IT MATTER!

PATRA P.K. AUTOIMMUNITY IN WISKOTT-ALDRICH SYNDROME: AN UNDEREXPLORED AREA

PECORARO A. EFFICACY AND SAFETY OF A NEW 16% SUBCUTANEOUS IMMUNOGLOBULIN PREPARATION IN A COHORT OF ADULT PRIMARY ANTIBODY DEFICIENCY PATIENTS

PÉREZ DE DIEGO R. DOUBLE-STRAND BREAK REPAIR THROUGH HOMOLOGOUS RECOMBINATION IN AUTOSOMAL RECESSIVE BCL10 DEFICIENCY 

PERGENT M. PID PRINCIPLES OF CARE – GLOBAL STATUS OF IMPLEMENTATION

PERGENT M. SOCIAL RIGHTS FOR PATIENTS WITH PID AND THEIR FAMILY IN FRANCE: A SOCIAL OBSERVATORY TO MAKE THE POINT

PHAN N.L.A. CASE SERIES REPORT OF COMMON VARIABLE IMMUNE DEFICIENCY : A SINGLE – INSTITUTION STUDY AT THE CHILDREN’S HOSPITAL 1, HO CHI MINH, VIETNAM

PITTROW D. FACILITATED IMMUNOGLOBULIN ADMINISTRATION REGISTRY AND OUTCOMES STUDY: INTERIM RESULTS

PONTES CUNHA DE CASTRO M.E. CLINICAL AND GENETIC CHARACTERISTICS OF PATIENTS WITH WISKOTT-ALDRICH SYNDROME IN BRAZIL

PREVOT J. INCLUSION OF PRIMARY IMMUNODEFICIENCIES IN WHO LIST OF ESSENTIAL DIAGNOSTICS

QUEK M.C. CASE REPORT OF HYPER IGM SYNDROME IN DOWN SYNDROME CHILD

RAEI N. A CASE REPORT OF SEVERE CONGENITAL NEUTROPENIA, A NOVEL HAX1 MUTATION

RAJ R. NOVEL PRETRANSPLANT IMMUNESUPPRESSION TO PREVENT GRAFT REJECTION IN PRIMARY IMMUNE DEFICIENCY DISORDERS

RAWAT A. INBORN ERRORS OF IMMUNITY: TWO AND HALF DECADE OF EXPERIENCE FROM A SINGLE CENTRE IN NORTH INDIA

RAWAT A. TARGETED NEXT GENERATION SEQUENCING FOR PRIMARY IMMUNODEFICIENCY DISEASES AT A TERTIARY CARE CENTRE FROM NORTH INDIA

RAYZAN E. TWINS WITH NOVEL X-LINKED VARIANT IN IL2RG GENE SUSPECTED TO EARLY ONSET INFLAMMATORY BOWEL DISEASE

RENTERIA VALDIVIEZO C.A. SEVERE CRYPTOCOCCAL INFECTION DUE TO ANTI-GRANULOCYTE-MACROPHAGE COLONY- STIMULATING FACTOR AUTOANTIBODIES

RIKHI R. FATAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS AS THE PRESENTING MANIFESTATION OF WISKOTT ALDRICH SYNDROME: A CASE REPORT

RIVALTA B. IMMUNOLOGICAL ANOMALIES IN PATIENTS WITH NOONAN SYNDROME AND RELATED DISORDERS

RIVERS L. INTERLEUKIN-18 IS A SENSITIVE MARKER OF INFLAMMATION IN WISKOTT ALDRICH SYNDROME

ROJAVIN M. PROSPECTIVE OPEN-LABEL SINGLE-ARM PHASE 3 STUDY OF THE SAFETY OF PRIVIGEN® IN JAPANESE PATIENTS WITH PRIMARY IMMUNODEFICIENCY

ROJAVIN M. PHARMACOKINETIC ANALYSIS OF 3-WEEKLY OR 4-WEEKLY INFUSIONS OF IGPRO10 IN JAPANESE PATIENTS WITH PRIMARY IMMUNODEFICIENCY

ROJAVIN M. STUDY DESIGN OF AN OPEN-LABEL MULTICENTER STUDY TO EVALUATE TOLERABILITY OF ACCELERATED SUBCUTANEOUS INFUSION OF IGPRO20: HIZENTRA LABEL OPTIMIZATION (HILO) STUDY

RUNKEN M. REAL WORLD INFECTION RATES BETWEEN INTRAVENOUS IMMUNOGLOBULINS IN PATIENTS WITH PRIMARY IMMUNODEFICIENCY DISEASE

SABR Z. SEVER VIRAL MENINGOENCEPHALITIS IN A PATIENT WITH PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY

SACHSENMAIER C. EPIGENETIC IMMUNE CELL QUANTIFICATION – A NOVEL APPROACH TO EARLY DETECTION OF PRIMARY IMMUNODEFICIENCY FROM DRIED BLOOD SPOTS

SAGHAFI S. PRENATAL DIAGNOSIS OF HYPER IMMUNOGLOBULIN E SYNDROME IN A FAMILY WITH DOCK8 DEFICIENCY HISTORY

SAHU S. SIIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 3(STAT3) LOSS OF FUNCTION RELATED AUTOSOMAL DOMINANT HYPER IGE SYNDROME AND OSTEOCLASTOGENESIS: STUDY OF THE OSTEO-IMMUNOLOGICAL CROSSTALK

SAIDANI K. COMMON VARIABLE IMMUNODEFICIENCY: CLINICAL AND IMMUNOLOGICAL PROFILE OF ALGERIAN PATIENTS

SALOKHIDDINOV M. CLINICAL EVALUATION RESPIRATORY IMPAIRMENT AND IMMUNOLOGICAL MANAGEMENT OF COMMON VARIABLE IMMUNODEFICIENCY DISORDERS

SCHIAFFINO T. CLINICAL AND GENETIC SPECTRUM OF PATIENTS WITH GATA2 MUTATIONS

SEIF F. A CASE WITH A NOVEL HOMOZYGOUS MUTATION IN OTULIN ACCOMPANIED BY AUTO-INFLAMMATION

SGRULLETTI M. EFFECTIVENESS OF IMMUNOMODULANT INTRAVENOUS IMMUNOGLOBULIN THERAPY IN A PATIENT WITH X-LINKED LYMPHOPROLIFERATIVE SYNDROME TYPE 2 (XLP-2)

SHA A. DISEASE BURDEN FOR PATIENTS WITH PRIMARY IMMUNODEFICIENCY DISEASES – EVIDENCE FROM SOUTH INDIA

SHABANI M. CONGENITAL CARDIAC DEFECTS IN G6PC3 DEFICIENCY; REPORT OF A NOVEL MUTATION AND A LITERATURE REVIEW

SHARMA A. HEMIPARESIS, SEIZURES AND ALTERED BEHAVIOUR IN A BOY WITH HYPOGAMMAGLOBULINEMIA: A DIAGNOSTIC AND THERAPEUTIC CHALLENGE

SHARMA J. COMMON VARIABLE IMMUNODEFICIENCY (CVID) LIKE PRESENTATION IN A YOUNG INDIAN PATIENT WITH NOVEL MUTATION IN DOCK2 GENE

SHARMA M. PRENATAL DIAGNOSIS AND CARRIER SCREENING FOR PRIMARY IMMUNODEFICIENCY DISEASES

SHARMA M. INTERPRETING NOVEL VARIANTS ON NEXT GENERATION SEQUENCING IN PRIMARY  IMMUNODEFICIENCY DISORDERS: OUR TRIALS AND TRIBULATIONS AT CHANDIGARH, NORTH INDIA

SHELLER R. EXPANDING THE REACH OF SEVERE COMBINED IMMUNODEFICIENCY TESTING: THE SCID NEWBORN SCREENING IMPLEMENTATION EXPERIENCE IN THE UNITED STATES

SHOKRI S. COMMON VARIABLE IMMUNODEFICIENCY AND LYMPHOMA, A CHICKEN AND EGG SITUATION

SINHA S. SKEWING OF SODIUM ANTIMONY GLUCONATE MEDIATED THERAPY FOR A PREDOMINANT PROTECTIVE T CELL RESPONSE DURING SCID-VISCERAL LEISHMANIASIS COINFECTION

SIZYAKINA L.P. THE POSSIBILITIES OF INCREASING THE EFFECTIVENESS OF REPLACEMENT THERAPY IN THE PRIMARY DEFECT OF ANTIBODY PRODUCTION

SOBOCINSKA A. ALLERGIC DISEASES IN PATIENTS WITH PRIMARY IMMUNODEFICIENCY

SOGKAS G. A NOVEL HETEROZYGOUS IKBA MUTATION, REPLACING SERINE AT POSITION 36, RESULTS IN COMBINED IMMUNODEFICIENCY WITHOUT EDA

SOLIS L. SWITCHING OF IMMUNOGLOBULIN THERAPIES: AN INTERNATIONAL SURVEY ON PATIENTS WITH PRIMARY IMMUNODEFICIENCIES

SUDHAKAR M. OSTEOMYELITIS A DREADED COMPLICATION OF CHRONIC GRANULOMATOUS DISEASE: EXPERIENCE FROM A TERTIARY CARE CENTER IN NORTH-WEST INDIA

SUDHAKAR M. PROLONGED EVENT FREE SURVIVAL IN 3 CHILDREN WITH AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME: A CLINICAL EXPERIENCE FROM A TERTIARY CARE CENTRE AT CHANDIGARH, NORTH INDIA.

TANTOU S. DIVERSE IMMUNOLOGICAL FINDINGS IN TWO SIBLINGS DIAGNOSED WITH ITCH DEFICIENCY

TANTOU S. COMMON VARIABLE IMMUNODEFICIENCY DIAGNOSED IN A 12 YEAR -OLD GIRL WITH GROWTH DELAY

TORRE M.G. RAPID RESPONSE OF CVID SKIN GRANULOMATOUS DISEASE TO INFLIXIMAB

TOWNSEND K. ANTIBODY RESPONSE TO PREVNAR13 IN IGG SUBCLASS DEFICIENT PATIENTS

ULAF R. CHRONIC MUCOCUTANEOUS CANDIDIASIS COMPLICATED BY ENDOFTALMITE – CASE REPORT

VALIYAGATH A. PRIMARY IMMUNODEFICIENCY IN INFECTION-PRONE CHILDREN : CLINICAL CHARACTERISTICS AND IMMUNOLOGICAL FINDINGS

VAN DER HOUWEN T. ENHANCED TLR5 EXPRESSION IN PATHERGY POSITIVE BEHÇET’S DISEASE PATIENTS INDICATES AN INNATE DRIVEN IMMUNE RESPONSE

VAN HAGEN P. INTERIM ANALYSIS OF A POSTAUTHORIZATION SAFETY STUDY ON THE LONG-TERM SAFETY OF HYALURONIDASE-FACILITATED SUBCUTANEOUS IMMUNOGLOBULIN 10% IN PATIENTS WITH PRIMARY IMMUNODEFICIENCY DISEASES IN EUROPE

VAN LAAR J. UNPRECEDED INFLUX OF HLH IN A TERTIARY REFERENCE CENTER

VENAVIDES W. A RARE PRIMARY IMMNUNODEFICIENCY: SELECTIVE IGM DEFICIENCY, CASE REPORT IN PEDIATRIC

VERAMENDI ESPINOZA L. NEONATAL DIARRHEA AND ECZEMA: FIRST PERUVIAN REPORTED CASE OF IMMUNE DYSREGULATION, POLYENDOCRINOPATHY, ENTEROPATHY, X-LINKED (IPEX) SYNDROME

VLAGEA A. DIHYDRORHODAMINE  FLOW CYTOMETRIC TEST  -APPLICATION IN TOLL-IL1R DEFICIENCIES-

WALTERS E. A CASE OF UNUSUAL SEVERE TUBERCULOSIS IN A CHILD WITH A VARIANT OF UNKNOWN SIGNIFICANCE OF THE IFN-GAMMA RECEPTOR 1: WIDENING THE SPECTRUM OF MENDELIAN SUSCEPTIBILITY TO TUBERCULOSIS?

WARNATZ K. RAPID PUSH INFUSION – A WELL-TOLERATED METHOD FOR SUBCUTANEOUS SELF-INJECTIONS OF GAMMANORM®: A RANDOMIZED NON-INFERIORITY CROSS-OVER TRIAL IN ADULT PATIENTS WITH PRIMARY IMMUNODEFICIENCIES

WOLSKA-KUSNIERZ B. 2ND POLISH NBS MEETING – A STEP TOWARD TRANSLATIONAL MEDICINE.

WORKMAN S. IMPACT OF IMMUNOGLOBULIN REPLACEMENT THERAPY SUPPLY INTERRUPTION: A SINGLE CENTRE PERSPECTIVE

YAILIAN A. SECURING IMMUNOGLOBULIN SUPPLY IN PRIMARY IMMUNODEFICIENCY AS A PRIORITY INDICATION: PATIENT’S CARE PATHWAY APPROACH

ZAFRA-TANAKA J. DOCTORS’ AWARENESS OF PRIMARY IMMUNODEFICIENCIES AT A REFERRAL CENTER, LIMA – PERU

ZANGARI P. NOVEL COMPOUND HETEROZYGOUS MUTATIONS IN IL-7 RECEPTOR ALPHA GENE IN A 15 MONTHS OLD GIRL PRESENTING WITH THROMBOCYTOPENIA AND NORMAL T CELL COUNT

ZEA-VERA A.F. EXPERIENCE OF THE CLINICAL IMMUNOLOGY SERVICE OF A PUBLIC UNIVERSITY HOSPITAL IN CALI, COLOMBIA

ZONDAG T. A RARE RAB27A VARIANT ASSOCIATED WITH A CASE OF HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS ALTERS EFFECTOR PROTEIN BINDING AFFINITIES