Search Results - "LESSI, M"

Encysted metacercariae of family Heterophyidae in infected fish in Dakahlia Governorate, an endemic focus in Egypt by Hegazi, Mai A, Hassan, Aisha T, Al-Nashar, Thanaa M, Abo-Elkheir, Omaima I, El-Lessi, Fatma M

“…The study re-evaluated the status of encysted metacercariae (EMC) of Family Heterophyidae in fresh and brackish water fish in an endemic focus in Egypt, as…”
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OS04-03 Unravelling the impact of endocrine disruptors on human neurodevelopment through the lens of brain organoids by Lessi, M., Caporale, N., Rigoli, M.T., Cheroni, C., Stucchi, S., Matassa, G., Bulgheresi, D., Valenti, A., Testa, G.

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Increased interferon‐gamma (IFN‐γ) levels produced in vitro by alloactivated T lymphocytes in systemic sclerosis and Raynaud's phenomenon by MOLTENI, M., DELLA BELLA, S., MASCAGNI, B., BAZZI, S., ZULIAN, C., COMPASSO, S., LESSI, M., SCORZA, R.

“…The aim of the present study was to analyse the in vitro proliferation and cytokine production by alloantigen‐stimulated peripheral blood mononuclear cells…”
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Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac disease by GIORDANO, M., BOLOGNESI, E., D'ALFONSO, S., LESSI, M., ZAVATTARI, P., ODERDA, G., CLOT, F., PERCOPO, S., CASARI, G., GRECO, L., TOSI, R., MOMIGLIANO-RICHIARDI, P.

“…Coeliac disease (CD) is a multigenic and multifactorial enteropathy triggered by gluten-composing proteins. A possible involvement of the intestinal…”
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Detection of AGXT gene mutations by denaturing high-performance liquid chromatography for diagnosis of hyperoxaluria type 1 by PIRULLI, D, GIORDANO, M, MOMIGLIANO-RICHIARDI, P, SAVOLDI, S, AMOROSO, A, LESSI, M, SPANO, A, PUZZER, D, ZEZLINA, S, BONIOTTO, M, CROVELLA, S, FLORIAN, F, MARANGELLA, M

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A variation in a Pit-1 site in the growth hormone gene (GH1) promoter induces a differential transcriptional activity by Giordano, Mara, Godi, Michela, Giacopelli, Francesca, Lessi, Monica, Mellone, Simona, Paracchini, Roberta, Petri, Antonella, Bellone, Jaele, Ravazzolo, Roberto, Bona, Gianni, Momigliano-Richiardi, Patricia

“…The proximal promoter of the human growth hormone gene (GH1) is highly polymorphic. We tested if promoter haplotypes differing at possibly functional sites,…”
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Detection of AGXT gene mutations by denaturing high-performance liquid chromatography for diagnosis of hyperoxyluria type 1 by Pirulli, D., Giordano, M., Lessi, M., Spanò, A., Puzzer, D., Zezlina, S., Boniotto, M., Crovella, S., Florian, F., Marangella, M., Momigliano-Richiardi, P., Savoldi, S.

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Detection of AGXT bgene mutations by denaturing high-performance liquid chromatography for diagnosis of hyperoxaluria type 1 by Pirulli, D, Giordano, M, Lessi, M, Spanò, A, Puzzer, D, Zezlina, S, Boniotto, M, Crovella, S, Florian, F, Marangella, M, Momigliano-Richiardi, P, Savoldi, S, Amoroso, A

“…Primary hyperoxaluria type 1 is an autosomal recessive disorder of glyoxylate metabolism, caused by a deficiency of alanine:glyoxylate aminotransferase, which…”
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Male Infertility by Niederberger, Craig Stuart, MD, FACS, Ohlander, Samuel John, MD, Pagani, Rodrigo Lessi, MD

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