16P Subtelomeric Duplication With Vascular Anomalies: An Albanian Case Report And Literature Review von Babameto-Laku, A., Mokini, V., Kuneshka, N., Sallabanda, S., Ylli, Z.

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Molecular Genetic Characterization of β-Thalassemia and Sickle Cell Syndrome in the Albanian Population von Babameto-Laku, A, Mitre, A, Berisha, S, Mokini, V, Roko, D

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Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping von Dib, C, Belal, S, Cohen, D, Novelli, G, Reutenauer, L, Ben Hamida, C, Mandel, J.-L, Linder, C, Vignal, A, Gyapay, G, Doerflinger, N, Hentati, F, Mokini, V, Kœnig, M, Le Paslier, D, Ben Hamida, M, Pandolfo, M

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The adolescent with acute renal failure and left ventricular hypertrophy in the absence of hypertension von BARBULLUSHI, M, THERESKA, N, PETRELA, M, IDRIZI, A, BUDO, L, RESULI, M, MOKINI, V

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Brachycephalosyndactyly with ptosis, cataract, colobomas, and linear areas of skin depigmentation von Mingarelli, R, Mokini, V, Castriota Scanderbeg, A, Dallapiccola, B

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Molecular pathology and haplotype analysis of Wilson disease in Mediterranean populations von FIGUS, A, ANGIUS, A, DE VIRGILIIS, S, LILLIU, F, FARCI, A. M. G, NURCHI, A, GIACCHINO, R, BARABINO, A, MARAZZI, M, ZANCAN, L, GREGGIO, N. A, MARCELLINI, M, LOUDIANOS, G, SOLINAS, A, DEPLANO, A, BARBERA, C, DEVOTO, M, OZSOYLU, S, KOCAK, N, AKAR, N, KARAYALCIN, S, MOKINI, V, CULLUFI, P, BERTINI, C, BALESTRIERI, A, CAO, A, PIRASTU, M, DESSI, V, LOI, A, DEIANA, M, LOVICU, M, OLLA, N, SOLE, G

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Analysis of 14 cystic fibrosis mutations in five South European populations von NUNES, V, GASPARINI, P, CIKULI, M, MOKINI, V, KOMEL, R, DALLAPICCOLA, B, PIGNATTI, P. F, LOUKOPOULOS, D, CASALS, T, ESTIVILL, X, NOVELLI, G, GAONA, A, BONIZZATO, A, SANGIUOLO, F, BALASSOPOULOU, A, GIMENEZ, F. J, DOGNINI, M, RAVNIK-GLAVAC, M

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Molecular Genetic Characterization of [beta]-Thalassemia and Sickle Cell Syndrome in the Albanian Population von Babameto-Laku, A, Mitre, A, Berisha, S, Mokini, V, Roko, D

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Effect of oxidants and antioxidants on chromosomal breakage in Fanconi anemia lymphocytes von DALLAPICCOLA, B, PORFIRIO, B, MOKINI, V, ALIMENA, G, ISACCHI, G, GANDINI, E

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THE CYSTIC-FIBROSIS DELTA-F508 MUTATION IN THE ALBANIAN POPULATION von NOVELLI, G, SANGIUOLO, F, MOKINI, CIKULI, M, PIAZZA, A, DALLAPICCOLA, B

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Failure of diepoxybutane to enhance sister chromatid exchange levels in Fanconi's anemia patients and heterozygotes von Porfirio, B, Dallapiccola, B, Mokini, V, Alimena, G, Gandini, E

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16p subtelomeric duplication with vascular anomalies: an Albanian case report and literature review von Babameto-Laku, A, Mokini, V, Kuneshka, N, Sallabanda, S, Ylli, Z

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Brachycephalosyndactyly with ptosis, cataract, colobomas, and linear areas of skin depigmentation von Mingarelli, R, Mokini, V, Castriota Scanderbeg, A, Dallapiccola, B

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Pain control with ultrasound-guided inguinal field block compared with spinal anesthesia after hernia surgery: A randomized trial von Mokini, Zhirajr, MD, Vitale, Giovanni, MD, Aletti, Gabriele, MD, Sacchi, Valentina, MD, Mauri, Tommaso, MD, Colombo, Valentina, MD, Fumagalli, Roberto, MD, Pesenti, Antonio, MD

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