Diagnostic and therapeutic uses of metaiodobenzylguanidine.

Por Parisi, M T, Hattner, R S
Publicado em 1992

The Drosophila pumilio gene encodes two functional protein isoforms that play multiple roles in germline development, gonadogenesis, oogenesis and embryogenesis.

Por Parisi, M, Lin, H
Publicado em 1999

Evaluation of new rapid commercial enzyme immunoassay for detection of Cryptosporidium oocysts in untreated stool specimens.

Por Parisi, M T, Tierno, P M
Publicado em 1995

The Effect of Hypertonic Media on Water Permeability of Frog Urinary Bladder : Inhibition by catecholamines and prostaglandin E(1)

Por Ripoche, P., Bourguet, J., Parisi, M.
Publicado em 1973

A human mitochondrial transcriptional activator can functionally replace a yeast mitochondrial HMG-box protein both in vivo and in vitro.

Por Parisi, M A, Xu, B, Clayton, D A
Publicado em 1993

The association between fibromyalgia and carpal tunnel syndrome in the general population.

Por Cimmino, M A, Parisi, M, Moggiana, G, Accardo, S
Publicado em 1996

Prevalence of rheumatoid arthritis in Italy: the Chiavari study

Por Cimmino, M., Parisi, M., Moggiana, G., Mela, G., Accardo, S.
Publicado em 1998

Evidence for redundancy but not trans factor-cis element coevolution in the regulation of Drosophila Yp genes.

Por Piano, F, Parisi, M J, Karess, R, Kambysellis, M P
Publicado em 1999

Plasma and urine neutrophil gelatinase-associated lipocalin in septic and nonseptic ICU patients

Por Vrettou, CS, Kokkoris, S, Apostolou, K, Parisi, M, Haritatos, E, Dimopoulos, S, Nanas, S
Publicado em 2012

Changes in skeletal muscle microcirculation after a hemodialysis session correlates with adequacy of dialysis

Por Pipili C, Grapsa E, Tripodaki ES, Ioannidou S, Manetos C, Parisi M, Nanas S
Publicado em 2015-06-01

The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndrome

Por PARISI, M., DINULOS, M. B., LEPPIG, K., SYBERT, V., ENG, C., HUDGINS, L.
Publicado em 2001

Actas de las segundas Jornadas de Astrofísica Estelar.

Por Jornadas de Astrofísica Estelar, Pintado, Olga I., Ahumada, Javier A., Parisi, M. Celeste, Palma, Tali
Publicado em 2011

Evaluation of microcirculation before and during continuous renal replacement therapy and the impact of dose prescription

Por Pipili, C, Vrettou, CS, Poulaki, S, Papastylianou, A, Parisi, M, Tripodaki, ES, Ioannidou, S, Kokkoris, S, Douka, E, Nanas, S
Publicado em 2012

Fibromyalgia and carpal tunnel syndrome

Por PEREZ-RUIZ, F, CALABOZO, M, ALONSO-RUIZ, A, RUIZ-LUCEA;, E, CIMMINO, M., PARISI, M., MOGGIANA, G., ACCARDO, S.
Publicado em 1997

AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndrome

Por Parisi, M A, Doherty, D, Eckert, M L, Shaw, D W W, Ozyurek, H, Aysun, S, Giray, O, Swaid, A Al, Shahwan, S Al, Dohayan, N, Bakhsh, E, Indridason, O S, Dobyns, W B, Bennett, C L, Chance, P F, Glass, I A
Publicado em 2006

Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)

Por Doherty, D, Parisi, M A, Finn, L S, Gunay-Aygun, M, Al-Mateen, M, Bates, D, Clericuzio, C, Demir, H, Dorschner, M, van Essen, A J, Gahl, W A, Gentile, M, Gorden, N T, Hikida, A, Knutzen, D, Özyurek, H, Phelps, I, Rosenthal, P, Verloes, A, Weigand, H, Chance, P F, Dobyns, W B, Glass, I A
Publicado em 2009