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Search Results - Larizza, Isabella S.
Search Results - Larizza, Isabella S.
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A peer support intervention in patients with hematologic malignancies undergoing hematopoietic stem cell transplantation (HSCT): The STEPP randomized pilot trial design and methods
by
Keane, Emma P.
,
Guo, Michelle
,
Gudenkauf, Lisa M.
,
Boardman, Annabella C.
,
Song, M. Tim
,
Wolfe, Emma D.
,
Larizza, Isabella S.
,
Mate-Kole, Manfred N.
,
Healy, Brian C.
,
Huffman, Jeff C.
,
El-Jawahri, Areej
,
Amonoo, Hermioni L.
Published in
Contemporary clinical trials
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A peer support intervention in patients with hematologic malignancies undergoing hematopoietic stem cell transplantation (HSCT): The STEPP randomized pilot trial design and methods...
by
Keane, Emma P.
,
Guo, Michelle
,
Gudenkauf, Lisa M.
,
Boardman, Annabella C.
,
Song, M. Tim
,
Wolfe, Emma D.
,
Larizza, Isabella S.
,
Mate-Kole, Manfred N.
,
Healy, Brian C.
,
Huffman, Jeff C.
,
El-Jawahri, Areej
,
Amonoo, Hermioni L.
Published in
Contemporary clinical trials
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Pathogenic Variants in STXBP1 and in Genes for GABAa Receptor Subunities Cause Atypical Rett/Rett-like Phenotypes
by
Cogliati, Francesca
,
Giorgini, Valentina
,
Masciadri, Maura
,
Bonati, Maria Teresa
,
Marchi, Margherita
,
Cracco, Irene
,
Gentilini, Davide
,
Peron, Angela
,
Savini, Miriam Nella
,
Spaccini, Luigina
,
Scelsa, Barbara
,
Maitz, Silvia
,
Veneselli, Edvige
,
Prato, Giulia
,
Pintaudi, Maria
,
Moroni, Isabella
,
Vignoli, Aglaia
,
Larizza, Lidia
,
Russo, Silvia
Published in
International journal of molecular sciences
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Molecular cytogenetics characterization of seven small supernumerary marker chromosomes derived from chromosome 19: Genotype-phenotype correlation and review of the literature
by
Recalcati, Maria Paola
,
Bonati, Maria Teresa
,
Beltrami, Nicola
,
Cardarelli, Laura
,
Catusi, Ilaria
,
Costa, Asia
,
Garzo, Maria
,
Mammi, Isabella
,
Mattina, Teresa
,
Nalesso, Elisa
,
Nardone, Anna Maria
,
Postorivo, Diana
,
Sajeva, Anna
,
Varricchio, Aminta
,
Verri, Annapia
,
Villa, Nicoletta
,
Larizza, Lidia
,
Giardino, Daniela
Published in
European journal of medical genetics
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Identification of sixty-two novel and twelve known FBN1 mutations in eighty-one unrelated probands with Marfan syndrome and other fibrillinopathies
by
Arbustini, Eloisa
,
Grasso, Maurizia
,
Ansaldi, Silvia
,
Malattia, Clara
,
Pilotto, Andrea
,
Porcu, Emanuele
,
Disabella, Eliana
,
Marziliano, Nicola
,
Pisani, Angela
,
Lanzarini, Luca
,
Mannarino, Savina
,
Larizza, Daniela
,
Mosconi, Mario
,
Antoniazzi, Elena
,
Zoia, M. Cristina
,
Meloni, Giulia
,
Magrassi, Lorenzo
,
Brega, Agnese
,
Bedeschi, Maria Francesca
,
Torrente, Isabella
,
Mari, Francesca
,
Tavazzi, Luigi
Published in
Human mutation
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Functional analysis of splicing mutations in exon 7 of NF1 gene
by
Bottillo, Irene
,
De Luca, Alessandro
,
Schirinzi, Annalisa
,
Guida, Valentina
,
Torrente, Isabella
,
Calvieri, Stefano
,
Gervasini, Cristina
,
Larizza, Lidia
,
Pizzuti, Antonio
,
Dallapiccola, Bruno
Published in
BMC medical genetics
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Functional analysis of splicing mutations in exon 7 of NF1gene
by
Bottillo, Irene
,
De Luca, Alessandro
,
Schirinzi, Annalisa
,
Guida, Valentina
,
Torrente, Isabella
,
Calvieri, Stefano
,
Gervasini, Cristina
,
Larizza, Lidia
,
Pizzuti, Antonio
,
Dallapiccola, Bruno
Published in
BMC medical genetics
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