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Results: 1-25 | 26-32
Results: 1-25/32
GENETIC-MAPPING OF A GENE RESPONSIBLE FOR A NEW RARE AUTOSOMAL-DOMINANT NEURONOPATHY
Authors: SERI M CUSANO R FORABOSCO P CAROLI F PICCO P BINI R MORRA VB LERONE M SILENGO M PELA I BORRONE C ROMEO G DEVOTO M
Citation: M. Seri et al., GENETIC-MAPPING OF A GENE RESPONSIBLE FOR A NEW RARE AUTOSOMAL-DOMINANT NEURONOPATHY, European journal of human genetics, 6, 1998, pp. 4138-4138
COMPLEX SPINAL MALFORMATION IN A 8-MONTH-OLD GIRL
Authors: ROMANENGO M FONDELLI MP PERRONE MV LAMBA LD CAMA A DIROCCO M BORRONE C
Citation: M. Romanengo et al., COMPLEX SPINAL MALFORMATION IN A 8-MONTH-OLD GIRL, Rivista italiana di pediatria, 24(2), 1998, pp. 322-324
DIFFERENCES IN TUMOR-NECROSIS-FACTOR-ALPHA SOLUBLE RECEPTOR SERUM CONCENTRATIONS BETWEEN PATIENTS WITH HENOCH-SCHONLEIN PURPURA AND PEDIATRIC SYSTEMIC LUPUS-ERYTHEMATOSUS - PATHOGENETIC IMPLICATIONS
Authors: GATTORNO M PICCO P BARBANO G STALLA F SORMANI MP BUONCOMPAGNI A GUSMANO R BORRONE C PISTOIA V
Citation: M. Gattorno et al., DIFFERENCES IN TUMOR-NECROSIS-FACTOR-ALPHA SOLUBLE RECEPTOR SERUM CONCENTRATIONS BETWEEN PATIENTS WITH HENOCH-SCHONLEIN PURPURA AND PEDIATRIC SYSTEMIC LUPUS-ERYTHEMATOSUS - PATHOGENETIC IMPLICATIONS, Journal of rheumatology, 25(2), 1998, pp. 361-365
COMPLICATIONS OF LYSINURIC PROTEIN INTOLERANCE MUST BE TREATED WITH IMMUNOSUPPRESSIVE DRUGS
Authors: DIROCCO M BUONCOMPAGNI A GATTON M PICCO P VIGNOLA S BORRONE C
Citation: M. Dirocco et al., COMPLICATIONS OF LYSINURIC PROTEIN INTOLERANCE MUST BE TREATED WITH IMMUNOSUPPRESSIVE DRUGS, Journal of inherited metabolic disease, 21(6), 1998, pp. 675-676
CUTANEOUS LEISHMANIASIS IN A 6-MONTH-OLD GIRL
Authors: DIROCCO M VIGNOLA S BORRONE C RAMPINI P OCCELLA C GAMBINI C
Citation: M. Dirocco et al., CUTANEOUS LEISHMANIASIS IN A 6-MONTH-OLD GIRL, The Journal of pediatrics, 132(4), 1998, pp. 748-748
SPECTRUM OF CLINICAL FEATURES ASSOCIATED WITH INTERSTITIAL CHROMOSOME22Q11 DELETIONS
Authors: DIROCCO M BUOCOMPAGNI A PICCO P VIGNOLA S BORRONE C GIMELLI G
Citation: M. Dirocco et al., SPECTRUM OF CLINICAL FEATURES ASSOCIATED WITH INTERSTITIAL CHROMOSOME22Q11 DELETIONS, Journal of Medical Genetics, 35(4), 1998, pp. 346-346
CLINICAL-FEATURES OF BEHCET-DISEASE IN ITALIAN CHILDREN
Authors: PICCO P BUONCOMPAGNI A GATTORNO M ALESSIO M BADO M FALCINI F FUGGETTA P GERLONI V LENORE L MEINI A SPROCATI M VIGNOLA S VIOLA S MARTINI A ZULIAN F BORRONE C
Citation: P. Picco et al., CLINICAL-FEATURES OF BEHCET-DISEASE IN ITALIAN CHILDREN, Arthritis and rheumatism, 41(9), 1998, pp. 1402-1402
ERYTHEMA MULTIFORME-LIKE MANIFESTATIONS AND ARTHRITIS IN A 3-YEAR-OLDCHILD WITH LEUKOCYTOCLASTIC VASCULITIS
Authors: GATTORNO M PICCO P GAMBINI C BUONCOMPAGNI A CASTAGNOLA E PISTOIA V BORRONE C
Citation: M. Gattorno et al., ERYTHEMA MULTIFORME-LIKE MANIFESTATIONS AND ARTHRITIS IN A 3-YEAR-OLDCHILD WITH LEUKOCYTOCLASTIC VASCULITIS, Clinical and experimental rheumatology, 15(3), 1997, pp. 329-332
BEHCETS-DISEASE IN CHILDREN
Authors: PICCO P GATTORNO M BUONCOMPAGNI A BORRONE C
Citation: P. Picco et al., BEHCETS-DISEASE IN CHILDREN, Rivista italiana di pediatria, 23(2), 1997, pp. 201-202
CASE-OF-THE-MONTH - A CHILD WITH STIFF NECK
Authors: DIROCCO M TASSO L FONDELLI MP MARINO C ROMANENGO M GIACCHINO R BORRONE C
Citation: M. Dirocco et al., CASE-OF-THE-MONTH - A CHILD WITH STIFF NECK, European journal of pediatrics, 156(9), 1997, pp. 737-738
RETINITIS-PIGMENTOSA, HYPOPITUITARISM, NEPHRONOPHTHISIS, AND MILD SKELETAL DYSPLASIA (RHYNS) - A NEW SYNDROME
Authors: DIROCCO M PICCO P ARSLANIAN A RESTAGNO G PERFUMO F BUONCOMPAGNI A GATTORNO M BORRONE C
Citation: M. Dirocco et al., RETINITIS-PIGMENTOSA, HYPOPITUITARISM, NEPHRONOPHTHISIS, AND MILD SKELETAL DYSPLASIA (RHYNS) - A NEW SYNDROME, American journal of medical genetics, 73(1), 1997, pp. 1-4
APPARENT PREFERENTIAL LOSS OF HETEROZYGOSITY AT TSC2 OVER TSC1 CHROMOSOMAL REGION IN TUBEROUS SCLEROSIS HAMARTOMAS
Authors: CARBONARA C LONGA L GROSSO E MAZZUCO G BORRONE C GARRE ML BRISIGOTTI M FILIPPI G SCABAR A GIANNOTTI A FALZONI P MONGA G GARINI G GABRIELLI M RIEGLER P DANESINO C RUGGIERI M MAGRO G MIGONE N
Citation: C. Carbonara et al., APPARENT PREFERENTIAL LOSS OF HETEROZYGOSITY AT TSC2 OVER TSC1 CHROMOSOMAL REGION IN TUBEROUS SCLEROSIS HAMARTOMAS, Genes, chromosomes & cancer, 15(1), 1996, pp. 18-25
AUTOIMMUNE-THYROIDITIS DEVELOPING INTO SYSTEMIC LUPUS-ERYTHEMATOSUS IN A 15-YEAR-OLD GIRL
Authors: PICCO P GATTORNO M BUONCOMPAGNI A PIAGGIO G STALLA F PISTOIA V BORRONE C
Citation: P. Picco et al., AUTOIMMUNE-THYROIDITIS DEVELOPING INTO SYSTEMIC LUPUS-ERYTHEMATOSUS IN A 15-YEAR-OLD GIRL, Clinical and experimental rheumatology, 14(3), 1996, pp. 348-349
VITAMIN-C-DEFICIENCY (SCURVY) IN PEDIATRI CS
Authors: PICCO P BUONCOMPAGNI A GATTORNO M BORRONE C TONETTI M CARBONE M OCCHI M GREMMO M
Citation: P. Picco et al., VITAMIN-C-DEFICIENCY (SCURVY) IN PEDIATRI CS, Rivista italiana di pediatria, 22(6), 1996, pp. 948-952
DIAGNOSTIC PROBLEMS IN CONGENITAL MYOTONIC-DYSTROPHY
Authors: DIROCCO M GENNARELLI M VENESELLI E BADO M ROMANENGO M CELLE ME CORDONE G BORRONE C
Citation: M. Dirocco et al., DIAGNOSTIC PROBLEMS IN CONGENITAL MYOTONIC-DYSTROPHY, European journal of pediatrics, 155(11), 1996, pp. 995-995
MOLECULAR-BASIS OF HEREDITARY FRUCTOSE INTOLERANCE IN ITALY - IDENTIFICATION OF 2 NOVEL MUTATIONS IN THE ALDOLASE-B GENE
Authors: SANTAMARIA R TAMASI S DELPIANO G SEBASTIO G ANDRIA G BORRONE C FALDELLA G IZZO P SALVATORE F
Citation: R. Santamaria et al., MOLECULAR-BASIS OF HEREDITARY FRUCTOSE INTOLERANCE IN ITALY - IDENTIFICATION OF 2 NOVEL MUTATIONS IN THE ALDOLASE-B GENE, Journal of Medical Genetics, 33(9), 1996, pp. 786-788
ARTHROGRYPOSIS, RENAL DYSFUNCTION AND CHOLESTASIS SYNDROME - REPORT OF 5 PATIENTS FROM 3 ITALIAN FAMILIES
Authors: DIROCCO M CALLEA F POLLICE B FARACI M CAMPIANI F BORRONE C
Citation: M. Dirocco et al., ARTHROGRYPOSIS, RENAL DYSFUNCTION AND CHOLESTASIS SYNDROME - REPORT OF 5 PATIENTS FROM 3 ITALIAN FAMILIES, European journal of pediatrics, 154(10), 1995, pp. 835-839
PRIMARY HYPOTHYROIDISM AS A CONSEQUENCE OF 131-I-METAIODOBENZYLGUANIDINE TREATMENT FOR CHILDREN WITH NEUROBLASTOMA
Authors: PICCO P GARAVENTA A CLAUDIANI F GATTORNO M DEBERNARDI B BORRONE C
Citation: P. Picco et al., PRIMARY HYPOTHYROIDISM AS A CONSEQUENCE OF 131-I-METAIODOBENZYLGUANIDINE TREATMENT FOR CHILDREN WITH NEUROBLASTOMA, Cancer, 76(9), 1995, pp. 1662-1664
ROLE OF BUSULFAN AND TOTAL-BODY IRRADIATION ON GROWTH OF PREPUBERTAL CHILDREN RECEIVING BONE-MARROW TRANSPLANTATION AND RESULTS OF TREATMENT WITH RECOMBINANT HUMAN GROWTH-HORMONE
Authors: GIORGIANI G BOZZOLA M LOCATELLI F PICCO P ZECCA M CISTERNINO M DALLORSO S BONETTI F DINI G BORRONE C REGAZZI MB DESTEFANO P SEVERI F
Citation: G. Giorgiani et al., ROLE OF BUSULFAN AND TOTAL-BODY IRRADIATION ON GROWTH OF PREPUBERTAL CHILDREN RECEIVING BONE-MARROW TRANSPLANTATION AND RESULTS OF TREATMENT WITH RECOMBINANT HUMAN GROWTH-HORMONE, Blood, 86(2), 1995, pp. 825-831
LOSS OF HETEROZYGOSITY AT TSC1 AND TSC2 LOCI IN TSC-ASSOCIATED AND SPORADIC HAMARTOMAS
Authors: CARBONARA C LONGA L GROSSO E MAZZUCCO G BORRONE C GARRE ML BRISIGOTTI M GIANNOTTI A FALZONI P MONGA G GARINI G GABRIELLI M RIEGLER P DANESINO C RUGGIERI M MAGRO G FILIPPI G SCABAR A BONETTI F PEA M MARTIGNONI G MIGNONE N
Citation: C. Carbonara et al., LOSS OF HETEROZYGOSITY AT TSC1 AND TSC2 LOCI IN TSC-ASSOCIATED AND SPORADIC HAMARTOMAS, American journal of human genetics, 57(4), 1995, pp. 321-321
IN-VIVO ACTIVATED T-LYMPHOCYTES FROM INSULIN-DEPENDENT DIABETES-MELLITUS (IDDM) PATIENTS DISPLAY HETEROGENEOUS EXPRESSION OF T-CELL RECEPTOR V-BETA AND CYTOKINE GENES
Authors: PRIGIONE I GHIOTTO F FACCHETTI P RINALDI GB SCARSO L PICCO P BORRONE C PISTOIA V
Citation: I. Prigione et al., IN-VIVO ACTIVATED T-LYMPHOCYTES FROM INSULIN-DEPENDENT DIABETES-MELLITUS (IDDM) PATIENTS DISPLAY HETEROGENEOUS EXPRESSION OF T-CELL RECEPTOR V-BETA AND CYTOKINE GENES, FCI. Fundamental and clinical immunology, 2(3), 1994, pp. 161-168
9Q34 LOSS OF HETEROZYGOSITY IN A TUBEROUS SCLEROSIS ASTROCYTOMA SUGGESTS A GROWTH SUPPRESSOR-LIKE ACTIVITY ALSO FOR THE TSC1 GENE
Authors: CARBONARA C LONGA L GROSSO E BORRONE C GARRE MG BRISIGOTTI M MIGONE N
Citation: C. Carbonara et al., 9Q34 LOSS OF HETEROZYGOSITY IN A TUBEROUS SCLEROSIS ASTROCYTOMA SUGGESTS A GROWTH SUPPRESSOR-LIKE ACTIVITY ALSO FOR THE TSC1 GENE, Human molecular genetics, 3(10), 1994, pp. 1829-1832
REFLEX SYMPHATETIC DYSTROPHY - DIFFICULTI ES IN DIAGNOSIS AND WAYS OFTREATMENT
Authors: BUONCOMPAGNI A PICCO P GREMMO M GATTORNO M CUTOLO M RONCARI P BORRONE C
Citation: A. Buoncompagni et al., REFLEX SYMPHATETIC DYSTROPHY - DIFFICULTI ES IN DIAGNOSIS AND WAYS OFTREATMENT, Rivista italiana di pediatria, 20(6), 1994, pp. 714-716
SJOGREN-LARSSON SYNDROME - NUCLEAR-MAGNETIC-RESONANCE IMAGING OF THE BRAIN IN A 4-YEAR-OLD BOY
Authors: DIROCCO M FILOCAMO M TORTORIDONATI P VENESELLI E BORRONE C RIZZO WB
Citation: M. Dirocco et al., SJOGREN-LARSSON SYNDROME - NUCLEAR-MAGNETIC-RESONANCE IMAGING OF THE BRAIN IN A 4-YEAR-OLD BOY, Journal of inherited metabolic disease, 17(1), 1994, pp. 112-114
INSULIN-LIKE GROWTH-FACTOR (IGF) IN CHILDREN WITH NEURAL-TUBE CLOSUREDEFECTS - A PRELIMINARY-REPORT
Authors: LEVERATTO L PICCO P CAMA A LAVIA N ROSSI G BARRECA A BORRONE C
Citation: L. Leveratto et al., INSULIN-LIKE GROWTH-FACTOR (IGF) IN CHILDREN WITH NEURAL-TUBE CLOSUREDEFECTS - A PRELIMINARY-REPORT, European journal of pediatric surgery, 3, 1993, pp. 19-20
Risultati: 1-25 | 26-32