Immunoglobulin injection for the treatment of multiple oral ulcers in Stevens–Johnson syndrome von Cicciù, M., Chiera, F., Gallizzi, R., Cicciù, A., Salpietro, C. D.

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Familial chronic nail candidiasis with ICAM-1 deficiency: a new form of chronic mucocutaneous candidiasis von Zuccarello, D, Salpietro, D C, Gangemi, S, Toscano, V, Merlino, M V, Briuglia, S, Bisignano, G, Mangino, M, Mingarelli, R, Dallapiccola, B

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Cadmium concentration in maternal and cord blood and infant birth weight: a study on healthy non-smoking women von Salpietro, C. D., Gangemi, S., Minciullo, P. L., Briuglia, S., Merlino, M. V., Stelitano, A., Cristani, M., Trombetta, D., Saija, A.

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Monocyte and neutrophil activity after minor surgical stress von Romeo, C., Cruccetti, A., Turiaco, A., Impellizzeri, P., Turiaco, N., Di Bella, C., Merlino, M.V., Cifalà, S., Basile, M., Gentile, C., Salpietro, D.C.

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A gene for familial isolated chronic nail candidiasis maps to chromosome 11p12–q12.1 von Mangino, M, Salpietro, D C, Zuccarello, D, Gangemi, S, Rigoli, L, Merlino, M V, Briuglia, S, Bisignano, G, Mingarelli, R, Dallapiccola, B

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Molecular analysis of sequence variants in the Fcε receptor Iβ gene and IL-4 gene promoter in Italian atopic families von RIGOLI, L, DI BELLA, C, PROCOPIO, V, BARBERIO, G, BARBERI, I, CAMINITI, L, LA GRUTTA, S, BRIUGLIA, S, SALPIETRO, C. D, PAJNO, G. B

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Linear scleroderma 'en coup de sabre' associated with facial atrophy in a patient seropositive for Borrelia burgdorferi: a true case of molecular mimicry? von Salpietro, D. C., Merlino, M. V., Bruglia, S., Guarneri, F., Vaccaro, M.

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Preliminary data suggest that mutations in the CgRP pathway are not involved in human sporadic cryptorchidism von Zuccarello, D, Morini, E, Douzgou, S, Ferlin, A, Pizzuti, A, Salpietro, D C, Foresta, C, Dallapiccola, B

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Allelic association of gene markers on chromosome 11q in Italian families with atopy von Rigoli, L, Salpietro, DC, Lavalle, R, Cafiero, G, Zuccarello, D, Barberi, I

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Protein carbonyl group content in patients affected by familiar chronic nail candidiasis von Gangemi, S, Saija, A, Tomaino, A, Cimino, F, Merendino, R A, Minciullo, P L, Briuglia, S, Merlino, M V, Dallapiccola, B, Ferlazzo, B, Salpietro, D C

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Serum levels of malondialdehyde and 4-hydroxy-2,3-nonenal in patients affected by familial chronic nail candidiasis von Gangemi, S, Saija, A, Minciullo, P L, Tomaino, A, Cimino, F, Bisignano, G, Briuglia, S, Merlino, M V, Dallapiccola, B, Salpietro, D C

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Epidemiology and Treatment of Otitis Media with Effusion in Children in the First Year of Primary School von Marchisio, P, Principi, N, Passali, D, Salpietro, D C, Boschi, G, Chetrì, G, Caramia, G, Longhi, R, Reali, E, Meloni, G, De Santis, A, Sacher, B, Cupido, G

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Serum Levels of Interleukin-18 in Splenectomized and Nonsplenectomized Thalassemic Patients: Preliminary Considerations von Gangemi, S., Merendino, R.A., Meo, A., Minciullo, P.L., Briuglia, S., Merlino, M.V., Rigoli, L., Tomasello, C., Salpietro, C.D.

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Mitochondrial DNA mutation at np 3243 in a family with maternally inherited diabetes mellitus von RIGOLI, L, SALPIETRO, D. C, CARUSO, R. A, CHIARENZA, A, BARBERI, I

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Reduced plasma c-AMP levels in children with atopic dermatitis von Salpietro, Damiano Carmelo, Naccari, Francesco, Polimeni, Lsabella, Pellegrino, Cristina

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Pain in neonatal intensive care: role of melatonin as an analgesic antioxidant von Gitto, Eloisa, Aversa, Salvatore, Salpietro, Carmelo Damiano, Barberi, Ignazio, Arrigo, Teresa, Trimarchi, Giuseppe, Reiter, Russel J., Pellegrino, Salvatore

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Confirmation of Nablus mask-like facial syndrome von Salpietro, Carmelo Damiano, Briuglia, Silvana, Rigoli, Luciana, Merlino, Maria Valeria, Dallapiccola, Bruno

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Hallerman-Streiff syndrome: Patient with decreased GH and insulin-like growth factor-1 von Damiano Salpietro, Carmelo, Briuglia, Silvana, Valeria Merlino, Maria, Piraino, Basilia, Valenzise, Mariella, Dallapiccola, Bruno

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Molecular analysis of β-thalassaemia patients in a high incidence area of southern Italy von Rigoli, L., Meo, A., Miceli, M.R., Alessio, K., Caruso, R.A., La Rosa, M.A., Salpietro, D.C., Ricca, M., Barberi, I.

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Distinguishing the four genetic causes of jouberts syndrome-related disorders von Valente, Enza Maria, Marsh, Sarah E., Castori, Marco, Dixon-Salazar, Tracy, Bertini, Enrico, Al-Gazali, Lihadh, Messer, Jean, Barbot, Clara, Woods, C. Geoffrey, Boltshauser, Eugen, Al-Tawari, Asma A., Salpietro, Carmelo D., Kayserili, Hulya, Sztriha, László, Gribaa, Moez, Koenig, Michel, Dallapiccola, Bruno, Gleeson, Joseph G.

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