Abstracts for poster presentation
Approved abstracts for poster presentation
IPIC2019 welcomed the submission of abstracts for original contributions to the field of clinical care of Primary Immunodeficiencies (PIDs) until July 14, 2019.
212 were approved for poster presentation and the 3 best posters have now been identified!
A full list of approved abstracts can be checked below.
List of approved abstracts
1st Place: Dr DEL PINO MOLINA, L. (Spain) – 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
2nd Place: Dr KARIM, F. (Netherlands) – CHRONIC SPONTANEOUS URTICARIA AS AUTO-IMMUNE FEATURE IN COMMON VARIABLE IMMUNODEFICIENCY
3rd Place: Dr RAKI SHIRZAD M. (Iran) – NEUTROPENIC PRIMARY IMMUNODEFICIENCY PATIENTS: A REGISTRY-BASED STUDY
Following posters ordered by presenter’s last name:
ABD EL-LATEEF H. SINGLETON-MERTEN SYNDROME;A RARE SYNDROMIC TYPE I INTERFERONOPATHY WITH AN EVOLVING AUTOIMMUNE DOMAIN (CASE REPORT)
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 |
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