ABERUMAND B. – UNDERSTANDING ATTITUDES AND OBSTACLES TO VACCINATION AGAINST COVID-19 IN PATIENTS WITH PRIMARY IMMUNODEFICIENCY

ADENAN A.M. – FUNCTIONAL EVALUATION OF NEUTROPHIL USING NITROBLUE TETRAZOLIUM TEST: 12 YEARS REVIEW IN A TERTIARY REFERRAL CENTRE IN MALAYSIA

AHMAD SHAWALUDIN M.Q. – A CASE REPORT CHRONIC MUCOCUTENOUS CANDIDIASIS  (CMCC) WITH MANIFESTATION OF RECURRENT INVASIVE STAPHYLOCOCCUS AUREUS INFECTION

ALBA CANO T. – ANTIBODY AND T-CELL RESPONSES FOLLOWING SARS-COV-2 VACCINATION IN PATIENTS WITH INBORN ERRORS OF IMMUNITY

ALEMAYEHU T. – CHALLENGES IN DIAGNOSING AUTO-INFLAMMATORY DISORDERS IN LOW RESOURCE SETTING

ANDREJEVIC S. – NINE-MONTH TREATMENT FOR A PATIENT WITH X-LINKED AGAMMAGLOBULINEMIA AND SARS-COV-2 INFECTION USING MULTIPLE THERAPEUTIC APPROACHES

AYGUN A. – IL12RB1 MUTATION PRESENTING WITH THE HYPER IG E SYNDROME PHENOTYPE

BAJAJ P. – NOVEL FERMT-3 GENE VARIANT IN A CHILD WITH LEUCOCYTE ADHESION DEFICIENCY TYPE-III.

BALASTEGUI H. – IDENTIFICATION OF A NOVEL NLRP12 VARIANT IN ASSOCIATION WITH A CASE OF SEVERE SARS-COV2 INFECTION

BALDRICH A. – DONOR-DERIVED T CELL IMMUNOGLOBULIN AND MUCIN DOMAIN 3 DEFICIENCY UNDERLYING POST-TRANSPLANT INFLAMMATORY BOWEL DISEASE

BASU S. – EARLY ONSET AMYLOIDOSIS IN COPA SYNDROME:FIRST CASE REPORT

BASU S. – BILATERAL CORNEAL ULCER IN PROLIDASE DEFICIENCY – A NOVEL ASSOCIATION

BHATTARAI D. – PROFILE OF INBORN ERRORS OF IMMUNITY (IEI) IN NEPAL- EVEREST AHEAD YET TO BE SCALED

BLANCO-LOBO P. – IN VITRO EFFECT OF RUXOLITINIB ON SIGNAL-TRANSDUCER-AND-ACTIVATOR-OF-TRANSCRIPTION 1 HYPERACTIVATION IN PATIENTS WITH DOMINANT NEGATIVE STAT3 MUTATIONS

BONDARENKO A. – GENETIC LANDSCAPE OF PRIMARY IMMUNODEFICIENCIES IN UKRAINE

BRODSZKI N. – REAL-WORLD SAFETY AND TOLERABILITY OF FACILITATED SUBCUTANEOUS IMMUNOGLOBULIN IN PEDIATRIC PATIENTS WITH PRIMARY IMMUNODEFICIENCY DISEASES: INTERIM ANALYSIS FROM A POST-AUTHORIZATION STUDY IN EUROPE

BUCCIOL G. – NOVEL IRF7 MUTATION IN A CHILD WITH RECURRENT PNEUMONIA

C. E. – EFFICACY AND SAFETY OF SUBCUTANEOUS HUMAN IMMUNOGLOBULIN (16.5%) IN PEDIATRIC PATIENTS WITH PRIMARY IMMUNODEFICIENCIES: DATA FROM TWO PHASE 3 STUDIES

CABAÑERO NAVALÓN M.D. – POTENTIAL ROLE OF ORAL, LUNG AND GASTROINTESTINAL MICROBIOTA IN THE PATHOPHYSIOLOGY OF COMMON VARIABLE IMMUNODEFICIENCY

CANTENYS MOLINA S. – CASE REPORT OF A POLYMORPHISM IN HOMOCYGOSIS IN THE MEFV GENE IN THE CONTEXT OF AN AUTOINFLAMMATORY SYNDROME

CARRABBA M. – HUMORAL RESPONSE TO ANTI-SARS-COV-2 VACCINATION IN PRIMARY ANTIBODY DEFICIENCIES PATIENTS

CAVALLO A. – SELECTIVE IMMUNOGLOBULIN A DEFICIENCY IN ASSOCIATION WITH BURKITT´S LYMPHOMA

CENGIZ H. – CASE REPORT: COMMON VARIABLE IMMUNE DEFICIENCY WITH THE SAME GENOTYPE AND TWO DIFFERENT CLINICS SEEN IN TWO SIBLINGS

CORNELISSEN H.M. – THE HAEMATOLOGICAL FEATURES OF PRIMARY IMMUNODEFICIENCY: A RETROSPECTIVE REVIEW OF THE ROUTINE LABORATORY INVESTIGATIONS OF THE SOUTH AFRICAN PRIMARY IMMUNODEFICIENCY REGISTRY

DAS J. – EVALUATION OF INBORN ERRORS OF IMMUNITY IN CHILDREN WITH SUSPECTED MENDELIAN SUSCEPTIBILITY TO MYCOBACTERIAL DISEASE

DE FELIPE B. – FIRST PROSPECTIVE PILOT STUDY OF SIMULTANEOUS NEONATAL SCREENING FOR SEVERE COMBINED IMMUNODEFICIENCIES AND SPINAL MUSCULAR ATROPHY

DE LA FUENTE MUNOZ E. – NOVEL STIM1 MUTATION

DELAFONTAINE S. – PATHOGENIC VARIANT IN TLR3 IN TWIN GIRLS WITH VIRAL ENCEPHALITIS AND OVERWHELMING INFLAMMATION

DHUNGEL S. – IMMUNOLOGICAL ABNORMALITIES IN CHILDREN PRESENTING WITH DISSEMINATED STAPHYLOCOCCUS INFECTION. A SINGLE UNIT EXPERIENCE FROM NORTH INDIA

DÍAZ M.D.L.M. – LATE DIAGNOSIS OF COMMON VARIABLE IMMUNODEFICIENCY (CVID): A PENDING PROBLEM

DÍAZ M.D.L.M. – CASE REPORT OF AUTOINMUNE THROMBOPENIA AND NEUTROPENIA IN ASSOCIATION TO AUTOINFLAMMATORY CLINICAL MANIFESTATIONS

DÍEZ J.M. – ANTIBODIES AGAINST COMMON HUMAN CORONAVIRUSES IN PLASMA AND IGG IMMUNOGLOBULIN MEDICINAL PRODUCTS

ERRAMI A. – MONOGENIC SUSCEPTIBILITY TO MYCOBACTERIAL DISEASES IN MOROCCAN PEDIATRIC PATIENTS

FERRANTI A.C. – CASE REPORT. NEW DIAGNOSTIC OF A 65-YEAR-OLD WOMAN WITH PAUCISYMPTOMATIC COMMON VARIABLE IMMUNODEFICIENCY (CVID) WITH VERY LOW LEVELS OF IGG (50 MG/DL), BUT NORMAL LEVELS OF IGA AND IGM

FERREIRA RAMOS B.C. – A FIRST LOOK AT THE NEWBORN SCREENING FOR INBORN ERRORS OF IMMUNITY IN SAO PAULO, BRAZIL

GAJARDO R. – HYPERIMMUNE IMMUNOGLOBULIN TO SARS-COV-2 HAS HIGH CAPACITY TO NEUTRALIZE WUHAN ORIGINAL WILD-TYPE VIRUS AND VIRUS VARIANTS OF CONCERN

GALLÓN DUQUE A. – SUBCUTANEOUS IMMUNOGLOBULIN REPLACEMENT THERAPY IN SECONDARY HYPOGAMMAGLOBULINEMIA DUE TO NEPHROTIC SYNDROME

GANGADHARAN H. – NEONATAL ONSET MULTISYSTEM INFLAMMATORY DISEASE (NOMID)- A SERIES OF TWO PATIENTS FROM A TERTIARY CARE CENTER IN NORTH INDIA

GANGADHARAN H. – PRIMARY IMMUNODEFICIENCY DISORDERS PRESENTING WITH AUTOIMMUNE MANIFESTATIONS IN THE ADULT INTERNAL MEDICINE WARD OF A TERTIARY CARE CENTRE IN SOUTH INDIA- A CASE SERIES

GARCIA-BUSTOS V. – INTEGRATING CLINICS, LABORATORY, AND IMAGING FOR THE DIAGNOSIS OF COMMON VARIABLE IMMUNODEFICIENCY-RELATED GRANULOMATOUS-LYMPHOCYTIC INTERSTITIAL LUNG DISEASE

GARCIA-MARTÍNEZ E. – IDENTIFICATION OF HETEROZYGOUS PSPIP1 AND WAS VARIANTS IN A PATIENT WITH RECURRENT INFECTIONS AND INFLAMMATORY-ASSOCIATED SYMPTOMS

GEBEYEHU N. – MENDELIAN SUSCEPTIBILITY TO MYCOBACTERIAL DISEASES IN A THIRTEEN YEAR OLD ETHIOPIAN GIRL WITH AUTOSOMAL DOMINANT INTERFERON GAMA RECEPTOR ONE DEFECT

GILL S. – QUANTITATIVE SERUM IMMUNOGLOBULIN AS AN ASSESSMENT OF ANTIBODIES DEFECT IN A TERTIARY REFERRAL CENTRE IN MALAYSIA

GLADIATOR A. – MANUAL ADMINISTRATION OF SUBCUTANEOUS IMMUNOGLOBULIN 20% IN CLINICAL PRACTICE IN PATIENTS WITH IMMUNODEFICIENCIES

GLADIATOR A. – TRANSITIONING SUBCUTANEOUS IMMUNOGLOBULIN 20% THERAPIES IN PATIENTS WITH PRIMARY AND SECONDARY IMMUNODEFICIENCIES: A CANADIAN REAL-WORLD STUDY

GOLWALA Z. – NON-TRAUMATIC FRACTURES AND OSTEOSARCOMA YEARS AFTER HAEMATOPOIETIC STEM CELL TRANSPLANTATION FOR PRIMARY IMMUNODEFICIENCY REVEAL UNEXPECTED DIAGNOSIS OF OSTEOGENESIS IMPERFECTA

GÓMEZ J. – HIGH DOSE IVIG IN SELECTED HIGH RISK PATIENTS WITH SEVERE COVID19 NEUMONIA

GÓMEZ-PÉREZ J. – GENOMIC RESULTS OF A PAEDIATRIC PATIENT WITH CENTRAL NERVOUS SYSTEM LYMPHOMA

GUISADO HERNÁNDEZ P. – TREATMENT OF AN IMMUNOLOGIC DOUBLE TROUBLE. JAK1/2INHIBITION IN CHILD WITH STAT1 GOF AND TRISOMY 21

HANITSCH L.G. – FACILITATED SUBCUTANEOUS IMMUNOGLOBULIN TREATMENT IN PATIENTS WITH PRIMARY AND SECONDARY IMMUNODEFICIENCIES: THE FIGARO STUDY

HOWLEY E. – EDUCATING AND EMPOWERING PATIENT FAMILIES THROUGH DIGITALLY DESIGNED INFORMATION UNIQUE TO THE EUROPEAN THYMUS TRANSPLANTATION PROGRAMME

IGBOEKWE E. – PEGYLATED RECOMBINANT ADENOSINE DEAMINASE (ELAPEGADEMASE) MAINTAINS DETOXIFICATION AND LYMPHOCYTE COUNTS IN PATIENTS WITH ADENOSINE DEAMINASE-DEFICIENT SEVERE COMBINED IMMUNODEFICIENCY

IJSPEERT H. – CLINICAL HETEROGENEITY IN A FAMILY WITH A GAIN-OF-FUNCTION VARIANT IN IKBKB: DOES SP110 FUNCTION AS A MODIFIER GENE?

IOAN A. – AUTOIMMUNITY AND AUTOINFLAMMATION IN ROMANIAN PRIMARY IMMUNODEFICIENCY PEDIATRIC PATIENTS: RETROSPECTIVE ANALYSIS

ITURRIETA-ZUAZO I. – SARS-COV-2 PNEUMONIA IN PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY: CLINICAL EXPERIENCE WITH CONVALESCENT PLASMA

JIMÉNEZ GARCIA C. – THE CHALLENGES OF DIAGNOSING PRIMARY IMMUNODEFICIENCY SPOTTED AFTER B-CELL LYMPHOPROLIFERATIVE MALIGNANCY

JINDAL A. – CLINICAL PROFILE OF A MULTICENTRE COHORT OF PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY (CVID) FROM INDIA

JINDAL A. – CLINICAL PROFILE OF A LARGE SINGLE CENTER COHORT OF HEREDITARY ANGIOEDEMA FROM NORTH INDIA

KARACA N. – MID-REGIONAL PROADRENOMEDULLIN (MR-PROADM) LEVELS IN PRIMARY IMMUNODEFICIENCIES COMPLICATED WITH PULMONARY MANIFESTATIONS

KARIM A. – IL-6 MEDIATED STAT3:NFKB SIGNALLING CASCADE IN LOSS OF FUNCTION STAT3 HYPER IGE SYNDROME PATIENT: CROSSTALK, DYNAMICS & SIGNAL INTEGEARTION

KASAP N. – A CASE OF STAT5B GOF WITH A NEW STAT5B MUTATION PRESENTING WITH TREATMENT-RESISTANT SEVERE ATOPIC DERMATITIS

KAUR A. – UTILITY OF MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION FOR DETECTING COPY NUMBER VARIATIONS IN PRIMARY IMMUNODEFICIENCY DISEASE

KAUR A. – GENETIC PROFILE OF HEREDITARY ANGIOEDEMA IN A SINGLE CENTRE COHORT FROM NORTH INDIA

KAUR S. – AIHA IN WISKOTT-ALDRICH SYNDROME

KHAN S.R. – SERUM IMMUNOGLOBULINS AND PNEUMONIA RISK AND LUNG FUNCTION IN MIDDLE-AGED AND ELDERLY INDIVIDUALS: A POPULATION-BASED STUDY

KHOREVA A. – EFFICACY AND SAFETY OF ROMIPLOSTIM IN TREATMENT OF THROMBOCYTOPENIA IN PATIENTS WITH WISKOTT-ALDRICH SYNDROME

KÖPPEN J. – COMBINED IMMUNODEFICIENCY IN A PATIENT WITH KABUKI SYNDROME

KOSTINOVA A. – HUMORAL IMMUNE RESPONSE AFTER ONE AND TWO DOSES OF ADJUVANTED INFLUENZA VACCINE IN PATIENTS WITH COMMON VARIABLE IMMUNE DEFICIENCY

LOGANATHAN S.K. – MALIGNANCIES  IN CHILDREN WITH INBORN ERRORS OF IMMUNITY – OUR EXPERIENCE AT CHANDIGARH, INDIA

LOPEZ MORENO N.V. – CONGENITAL NEUTROPENIA DUE TO HOMOZYGOUS MUTATION IN GLUCOSE-6-PHOSPHATASE CATALYTIC SUBUNIT 3 DIAGNOSED IN AN ADULT

LÓPEZ-NEVADO M. – A NOVEL PATIENT WITH COMPLETE STAT2 DEFICIENCY PRESENTED WITH HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS AND IMPAIRED IFN-A SIGNALING

LÓPEZ-NEVADO M. – NOVEL MUTATIONS IN THE TET2 GENE IN TWO UNRELATED PATIENTS WITH AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME-LIKE (ALPS-LIKE) PHENOTYPE AND SUSCEPTIBILITY TO HEMATOLOGIC MALIGNANCY

LÓPEZ-NEVADO M. – PRIMARY IMMUNE REGULATORY DISORDERS WITH AN AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME-LIKE PHENOTYPE: IMMUNOLOGIC EVALUATION, EARLY DIAGNOSIS, AND MANAGEMENT

LOTFY S. – A 14-YEAR-OLD BOY WITH SEVERE COMBINED IMMUNODEFICIENCY

MAHLAOUI N. – REAL-WORLD EVIDENCE IN PATIENTS WITH PRIMARY IMMUNO-DEFICIENCIES (PID): LEARNINGS FROM THE ECONOMHYQ STUDY, A FRENCH NATIONAL COHORT

MANDASARI A.A. – DIVERSE PHENOTYPES IN MICE CARRYING NOVEL LEU387ARG GAIN-OF-FUNCTION VARIANT IN SIGNAL TRANSDUCER ACTIVATOR TRANSCRIPTION 3

MARCUS N. – DEVELOPMENT OF A NOVEL BTK LENTIVIRAL VECTOR FOR GENE THERAPY OF X-LINKED AGAMMAGLOBULINEMIA

MARKELJ G. – A SLOVENIAN EXPERIENCE OF NETHERTON SYNDROME PATIENTS IN THE LAST 30 YEARS

MARKELJ G. – USE OF VIRUS SPECIFIC T CELLS FOR EBV+ LYMPHOPROLIFERATION PRETRANSPLANTATION IN AN ARPC1B DEFICIENT PATIENT

MASLE-FARQUHAR E. – OVERACTIVE STAT3 DRIVES ABERRANT ACCUMULATION OF AUTOIMMUNE-ASSOCIATED CD21LOW CD23LOW B CELLS

MEJÍA M. – NEUTRALIZING ANTIBODIES AFTER MRNA-1273 VACCINATION IN A COHORT OF PATIENTS WITH INBORN ERRORS OF IMMUNITY

MILITO C. – THE IMPACT OF SARS-COV-2 INFECTION IN PATIENTS WITH INBORN ERRORS OF IMMUNITY: THE EXPERIENCE OF THE ITALIAN NETWORK FOR PRIMARY IMMUNODEFICIENCY (IPINET)

MOHAMED MOHAMED K. – CELLULAR AND HUMORAL RESPONSES TO SARS-COV-2 VACCINE IN PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY

MONCAYO MUÑOZ A.P. – LONG-TERM SURVIVAL IN A PATIENT WITH COMMON VARIABLE IMMUNODEFICIENCY AFTER LUNG TRANSPLANTATION: POSSIBLE ROLE OF A HIGH-DOSE INTRAVENOUS IMMUNOGLOBULIN PROTOCOL

MOUNDIR A. – 10 YEARS OF MOROCCAN EXPERIENCE IN THE GENETIC DIAGNOSIS OF PRIMARY IMMUNODEFICIENCIES

MUNTEANU A.N. – EXTENDED LYMPHOCYTE IMMUNOPHENOTYPING FOR IMMUNODIAGNOSIS  OF RECURRENT RESPIRATORY INFECTIONS IN THE ABSENCE OF PRIMARY IMMUNODEFICIENCY

NAGY A. – LONG-TERM SAFETY OF FACILITATED SUBCUTANEOUS IMMUNOGLOBULIN: FINAL RESULTS FROM A POST-AUTHORIZATION STUDY

NASRULLAYEVA G. – SKIN DISORDERS AND IMMUNOLOGICAL FEATURES IN AZERBAIJANI PATIENTS WITH HYPER IGE SYNDROME

NDIAYE DIOP M.T. – DERMATOLOGICAL MANIFESTATIONS DURING PRIMARY IMMUNE DEFICIENCY IN DARK SKIN

NG K.F. – THE MULTIFACETED SYNDROMIC IMMUNODEFICIENCIES: A SINGLE INSTITUTION’S 15-YEAR EXPERIENCE

NIROUEI M. – MONOGENIC DISORDER ASSOCIATED WITH AUROIMMUNE LYMPHPPROLIFERATIVE SYNDROME -LIKE PHENOTYPE

O’FARRILL P. – COMMON VARIABLE IMMUNODEFICIENCY IN ADULTS PATIENTS AND LIVER DISORDERS

PALAZZO D. – GATA2 DEFICIENCY AND HIDRADENITIS SUPPURATIVA IN A YOUNG ADULT: A THERAPEUTIC CHALLENGE

PANG F. – PATIENT- AND CAREGIVER-REPORTED QUALITY OF LIFE AND BURDEN OF DISEASE IN WISKOTT-ALDRICH SYNDROME (WAS): FINDINGS FROM A MULTINATIONAL SURVEY

PUIG-NAVARRO C. – USE OF IMMUNOGLOBULIN REPLACEMENT THERAPY: REAL-LIFE EXPERIENCE OF AN  IMMUNODEFICIENCY UNIT

RAWAT A. – PITFALLS OF TARGETED NEXT GENERATION SEQUENCING FOR DIAGNOSIS OF INBORN ERRORS OF IMMUNITY: PRELIMINARY EXPERIENCE FROM A TERTIARY CARE CENTRE AT CHANDIGARH, NORTH INDIA

RIKHI R. – GENETIC PROFILE OF CHILDREN WITH AUTOIMMUNE MANIFESTATIONS IN WISKOTT-ALDRICH SYNDROME

ROBERTA A.D.P – SURVEY RESULTS FOR HEALTH PROFESSIONALS ON INBORN ERRORS OF IMMUNITY IN ARGENTINA

ROMERO C. – SURVEILLANCE OF ANTI-SARS-COV-2 ANTIBODIES IN HEALTHY DONORS PLASMA POOLS AND INTRAVENOUS IMMUNOGLOBULIN PRODUCTS. A CONTINOUS PROGRAM FROM MAY 2020

SACHSENMAIER C. – I.MUNE NEO – A NEW TEST FOR EPIGENETIC IMMUNE CELL QUANTIFICATION IN NEWBORNS

SANCHI – PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA (XLA) MAY HAVE T CELL PROLIFERATION ABNORMALITIES: OUR EXPERIENCE AT CHANDIGARH, INDIA

SANCHI – AUTOIMMUNE MANIFESTATIONS IN A LARGE MULTI-CENTRE COHORT OF PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY IN INDIA

SEALFON A. – A NOVEL APPROACH TO CUSTOMIZING THE FLOW PROFILE FOR THE ADMINISTRATION OF SUBCUTANEOUS IMMUNOGLOBINS FOR INDIVIDUAL INFUSIONS WITH BENEFITS TO MINIMIZE OR ELIMINATE SITE REACTIONS—A CASE STUDY

SEIF F. – GENETIC DEFECTS IN INNATE AND ADAPTIVE IMMUNITY

SEMERARO M. – SUSTAINED CLINICAL IMPROVEMENT IN THREE PATIENTS AFFECTED BY ACTIVATED PHOSPHOINOSITIDE 3-KINASE DELTA SYNDROME (APDS) TREATED BY THE SELECTIVE PI3KDELTA INHIBITOR LENIOLISIB

SERRA I. – ACTIVATED PI3K-DELTA SYNDROME, AN IMMUNODEFICIENCY DISORDER, LEADS TO SENSORIMOTOR DEFICITS RECAPITULATED IN A MURINE MODEL

SHA A. – MEASURING TREATMENT SATISFACTION IN PATIENTS WITH PRIMARY IMMUNODEFICIENCY DISEASES RECEIVING IMMUNOGLOBULIN INFUSIONS

SHARIFINEJAD N. – THE FIRST PATIENT FROM THE NATIONAL IRANIAN REGISTRY WITH PROTEIN KINASE C-DELTA DEFECT, AND REVIEW OF THE LITERATURE

SHARMA K. – CROSS-TALK BETWEEN NOX AND AUTOPHAGY TO MAINTAIN THE LONG-TERM B CELL MEMORY IN PATIENTS WITH CHRONIC GRANULOMATOUS DISEASE

SIDDIQUE S. – DISEASE BURDEN FOR PATIENTS WITH PRIMARY IMMUNODEFICIENCY DISEASES – A COMPARATIVE STUDY

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

SIL A. – UNUSUAL PRESENTATION OF AN UNCOMMON PRMARY IMMUNODEFICIENCY

SOLIS L. – PID LIFE INDEX: THE TOOL MEASURING THE GLOBAL PID ENVIRONMENT

SOLIS L. – SCREEN4RARE: ADVOCATING FOR IMPROVED EU COOPERATION IN THE FIELD OF NEONATAL SCREENING

SUDHAKAR M. – X-LINKED LYMPHOPROLIFERATIVE SYNDROME: EXPERIENCE FROM A TERTIARY CARE CENTER FROM NORTH INDIA

SUDHAKAR M. – DEFICIENCY OF ADENOSINE DEAMINASE 2: MYRIAD FACES IN A SINGLE FAMILY

SUDHAKAR M. – MONOGENIC AUTOIMMUNE HEMOLYTIC ANEMIA: EXPERIENCE FROM A TERTIARY CARE CENTER FROM NORTH INDIA

TABINI M. – NURSES MANAGEMENT OF PATIENTS WITH INBORN ERROR OF IMMUNITY DURING COVID-19 PANDEMIC IN MILAN, ITALY

TAHIAT A. – THE OCCURRENCE OF AUTOIMMUNE DISEASES IN ALGERIAN PATIENTS WITH HOMOZYGOUS MUTATIONS IN RAG1 AND RAG2

TEIXEIRA C. – HYPOGAMMAGLOBULINEMIA AND TRICHOTHIODISTROPHY: AN UNEXPECTED ASSOCIATION?

TOPYILDIZ E. – A NOVEL MUTATION IN A TURKISH CHILD PRESENTED WITH HIGH IGM LEVELS AT ADMISSION AND DIAGNOSED AS XLA FOR A LONG TIME

TROPPER L. – THE CARE-FOR-RARE CHILD LIFE SPECIALIST PROGRAM – A MODEL TO IMPLEMENT THE PRINCIPLES OF THE UNITED NATION CONVENTION ON CHILDREN’S RIGHTS INTO PEDIATRIC CLINICAL CARE

TYAGI R. – IS MORTALITY AVOIDABLE IN PATIENTS WITH HEREDITARY ANGIOEDEMA IN THE 21ST CENTURY?: A DEVELOPING COUNTRY PERSPECTIVE

TYAGI R. – GENETIC BASIS OF COMMON VARIABLE IMMUNODEFICIENCY (CVID): A MULTICENTRE EXPERIENCE FROM INDIA

VAN STIGT A. – SOLUBLE SURFACE MOLECULES IN SERUM SUGGEST INVOLVEMENT OF ACTIVATED T-CELLS AND MACROPHAGES IN NON-INFECTIOUS COMLICATIONS IN CVID

VARGAS CELY F.S. – SEVERE AUTOIMMUNITY TRAITS IN A COLOMBIAN BOY: A NOVEL NRAS MUTATION C.182A>G (P.Q61R) CAUSING RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISEASE

VARGAS CELY F.S. – AN UNUSUAL CASE OF HEPATOMEGALY, PANCYTOPENIA AND AUTOINFLAMMATORY SYNDROME IN A COLOMBIAN GIRL: ABOUT A CASE OF PSTPIP1-ASSOCIATED MYELOID-RELATED PROTEINEMIA INFLAMMATORY SYNDROME

VÁSQUEZ P. – ASYMPTOMATIC SARS COV-2 INFECTION IN A 59 YEAR OLD WOMAN WITH AN AUTOINFLAMMATORY DISEASE DUE TO SOMATIC NLRC4 MOSAICISM

VENAVIDES W. – X- LINKED LYMPHOPROLIFERATIVE SYNDROME -1: ONE CASE IN A MILLION

VILLEGAS SILES M.F. – “DE NOVO” DETECTION OF TOTAL IGM AFTER A SARS COV2 INFECTION IN A PATIENT WITH COMMON VARIABLE IMMUNODEFICIENCY

ZHOU Z.Z. – THREE PATIENTS WITH SEVERE DEFECTS IN INTERFERON GAMMA RECEPTOR SIGNALING: A CHALLENGING DIAGNOSIS