Works by Lalatta, Faustina

Results: 54

Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis.

Published in:

2010

By:

Lalatta, Faustina;
Quagliarini, Donatella;
Folliero, Emanuela;
Cavallari, Ugo;
Gentilin, Barbara;
Castorina, Pierangela;
Forzano, Francesca;
Forzano, Serena;
Grosso, Enrico;
Viassolo, Valeria;
Naretto, Valeria;
Gattone, Stefania;
Ceriani, Florinda;
Faravelli, Francesca;
Gargantini, Luigi;
Naretto, Valeria Giorgia

Publication type:

journal article

"Your son has Klinefelter syndrome." How parents react to a prenatal diagnosis.

Published in:

Children's Health Care, 2021, v. 50, n. 3, p. 324, doi. 10.1080/02739615.2021.1903325

By:

Zampini, Laura;
Dall'Ara, Francesca;
Silibello, Gaia;
Ajmone, Paola Francesca;
Monti, Federico;
Rigamonti, Claudia;
Lalatta, Faustina;
Costantino, Maria Antonella;
Vizziello, Paola Giovanna

Publication type:

Article

Partial Trisomy of 7q: Case Report and Literature Review.

Published in:

Journal of Child Neurology, 2008, v. 23, n. 5, p. 572, doi. 10.1177/0883073807309776

By:

Scelsa, Barbara;
Bedeschi, Francesca Maria;
Guerneri, Silvana;
Lalatta, Faustina;
Introvini, Paola

Publication type:

Article

Seizure and EEG Patterns in Angelman's Syndrome.

Published in:

Journal of Child Neurology, 1995, v. 10, n. 6, p. 467, doi. 10.1177/088307389501000609

By:

Viani, Francesco;
Romeo, Antonino;
Viri, Maurizio;
Mastrangelo, Massimo;
Lalatta, Faustina;
Selicorni, Angelo;
Gobbi, Giuseppe;
Lanzi, Giovanni;
Bettio, Daniela;
Briscioli, Vincenza;
Di Segni, Marina;
Parini, Rossella;
Terzoli, Gianluigi

Publication type:

Article

A new de novo missense mutation in connexin 26 in a sporadic case of nonsyndromic deafness.

Published in:

2007

By:

Primignani P;
Trotta L;
Castorina P;
Lalatta F;
Cuda D;
Murri A;
Ambrosetti U;
Cesarani A;
Curcio C;
Coviello D;
Travi M;
Primignani, Paola;
Trotta, Luca;
Castorina, Pierangela;
Lalatta, Faustina;
Cuda, Domenico;
Murri, Alessandra;
Ambrosetti, Umberto;
Cesarani, Antonio;
Curcio, Cristina

Publication type:

journal article

Fetal death associated with diffuse mesangial sclerosis combined with bilateral multicystic kidney.

Published in:

Case Reports in Perinatal Medicine, 2013, v. 2, n. 1/2, p. 33, doi. 10.1515/crpm-2012-0064

By:

Bellini, Martina;
Rizzuti, Tommaso;
Ardissino, Gianluigi;
Boito, Simona;
Fogliani, Roberto;
Lalatta, Faustina

Publication type:

Article

Prosodic features of maternal input to children with sex chromosome trisomies.

Published in:

First Language, 2022, v. 42, n. 5, p. 613, doi. 10.1177/01427237221098553

By:

Provera, Alessandra;
Zanchi, Paola;
Silibello, Gaia;
Dall'Ara, Francesca;
Rigamonti, Claudia;
Monti, Federico;
Ajmone, Paola Francesca;
Lalatta, Faustina;
Costantino, Maria Antonella;
Vizziello, Paola Giovanna;
Zampini, Laura

Publication type:

Article

Preverbal skills in 8-month-old children with sex chromosome trisomies.

Published in:

First Language, 2021, v. 41, n. 2, p. 200, doi. 10.1177/0142723720962944

By:

Zampini, Laura;
Burla, Tiziana;
Silibello, Gaia;
Capelli, Elena;
Dall'Ara, Francesca;
Rigamonti, Claudia;
Ajmone, Paola Francesca;
Monti, Federico;
Zanchi, Paola;
Lalatta, Faustina;
Costantino, Maria Antonella;
Vizziello, Paola Giovanna

Publication type:

Article

Banking together. A unified model of informed consent for biobanking.

Published in:

EMBO Reports, 2008, v. 9, n. 4, p. 307, doi. 10.1038/embor.2008.41

By:

Salvaterra, Elena;
Lecchi, Lucilla;
Giovanelli, Silvia;
Butti, Barbara;
Bardella, Maria Teresa;
Bertazzi, Pier Alberto;
Bosari, Silvano;
Coggi, Guido;
Coviello, Domenico A;
Lalatta, Faustina;
Moggio, Maurizio;
Nosotti, Mario;
Zanella, Alberto;
Rebulla, Paolo

Publication type:

Article

Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases.

Published in:

BMC Medical Genetics, 2017, v. 18, p. 1, doi. 10.1186/s12881-017-0470-z

By:

Bedeschi, Maria Francesca;
Calvello, Mariarosaria;
Paganini, Leda;
Pezzani, Lidia;
Baccarin, Marco;
Fontana, Laura;
Sirchia, Silvia M.;
Guerneri, Silvana;
Canazza, Lorena;
Leva, Ernesto;
Colombo, Lorenzo;
Lalatta, Faustina;
Mosca, Fabio;
Tabano, Silvia;
Miozzo, Monica

Publication type:

Article

Loss-of-Function FANCL Mutations Associate with Severe Fanconi Anemia Overlapping the VACTERL Association.

Published in:

Human Mutation, 2015, v. 36, n. 5, p. 562, doi. 10.1002/humu.22784

By:

Vetro, Annalisa;
Iascone, Maria;
Limongelli, Ivan;
Ameziane, Najim;
Gana, Simone;
Mina, Erika Della;
Giussani, Ursula;
Ciccone, Roberto;
Forlino, Antonella;
Pezzoli, Laura;
Rooimans, Martin A.;
Essen, Antoni J.;
Messa, Jole;
Rizzuti, Tommaso;
Bianchi, Paolo;
Dorsman, Josephine;
Winter, Johan P.;
Lalatta, Faustina;
Zuffardi, Orsetta

Publication type:

Article

Discordant prenatal phenotype and karyotype of monozygotic twins characterized by the unequal distribution of two cell lines investigated by different methods: a review.

Published in:

2008

By:

Gentilin, Barbara;
Guerneri, Silvana;
Bianchi, Vera;
Natacci, Federica;
Colombo, Augusto;
Fogliani, Roberto;
Fortuna, Renato;
Coviello, Domenico A.;
Curcio, Cristina;
Lalatta, Faustina

Publication type:

journal article

Impaired glucose metabolism in subjects with the Williams-Beuren syndrome: A five-year follow-up cohort study.

Published in:

PLoS ONE, 2017, v. 12, n. 10, p. 1, doi. 10.1371/journal.pone.0185371

By:

Lunati, Maria Elena;
Bedeschi, Maria Francesca;
Resi, Veronica;
Grancini, Valeria;
Palmieri, Eva;
Salera, Simona;
Lalatta, Faustina;
Pugliese, Giuseppe;
Orsi, Emanuela

Publication type:

Article

Familial Duplication/Deletion of 1q42.13q43 as Meiotic Consequence of an Intrachromosomal Insertion in Chromosome 1.

Published in:

2018

By:

Silipigni, Rosamaria;
Monfrini, Edoardo;
Baccarin, Marco;
Giangiobbe, Sara;
Lalatta, Faustina;
Guerneri, Silvana;
Bedeschi, Maria Francesca

Publication type:

Case Study

Prenatal ultrasound factors and genetic disorders in pregnancies complicated by polyhydramnios.

Published in:

2016

By:

Boito, Simona;
Crovetto, Francesca;
Ischia, Benedetta;
Crippa, Beatrice Letizia;
Fabietti, Isabella;
Bedeschi, Maria Francesca;
Lalatta, Faustina;
Colombo, Lorenzo;
Mosca, Fabio;
Fedele, Luigi;
Persico, Nicola

Publication type:

journal article

Prenatal and postnatal findings in five cases of Fryns syndrome.

Published in:

2014

By:

Peron, Angela;
Bedeschi, Maria Francesca;
Fabietti, Isabella;
Baffero, Giulia Maria;
Fogliani, Roberto;
Ciralli, Fabrizio;
Mosca, Fabio;
Rizzuti, Tommaso;
Leva, Ernesto;
Lalatta, Faustina

Publication type:

Other

Author's reply regarding 'Confined placental mosaicism at chorionic villous sampling: risk factors and pregnancy outcome'.

Published in:

Prenatal Diagnosis, 2013, v. 33, n. 3, p. 303, doi. 10.1002/pd.4046

By:

Baffero, Giulia Maria;
Somigliana, Edgardo;
Crovetto, Francesca;
Paffoni, Alessio;
Persico, Nicola;
Guerneri, Silvana;
Lalatta, Faustina;
Fogliani, Roberto;
Fedele, Luigi

Publication type:

Article

Confined placental mosaicism at chorionic villous sampling: risk factors and pregnancy outcome.

Published in:

Prenatal Diagnosis, 2012, v. 32, n. 11, p. 1102, doi. 10.1002/pd.3965

By:

Baffero, Giulia Maria;
Somigliana, Edgardo;
Crovetto, Francesca;
Paffoni, Alessio;
Persico, Nicola;
Guerneri, Silvana;
Lalatta, Faustina;
Fogliani, Roberto;
Fedele, Luigi

Publication type:

Article

Congenital diaphragmatic hernia as prenatal presentation of Apert syndrome.

Published in:

2011

By:

Bulfamante, Gaetano;
Gana, Simone;
Avagliano, Laura;
Fabietti, Isabella;
Gentilin, Barbara;
Lalatta, Faustina

Publication type:

Case Study

De novo balanced chromosome rearrangements in prenatal diagnosis.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 3, p. 257, doi. 10.1002/pd.2215

By:

Giardino, Daniela;
Corti, Cecilia;
Ballarati, Lucia;
Colombo, Daniela;
Sala, Elena;
Villa, Nicoletta;
Piombo, Giuseppe;
Pierluigi, Mauro;
Faravelli, Francesca;
Guerneri, Silvana;
Coviello, Domenico;
Lalatta, Faustina;
Cavallari, Ugo;
Bellotti, Daniela;
Barlati, Sergio;
Croci, Gianfranco;
Franchi, Fabrizia;
Savin, Elisa;
Nocera, Gianfranco;
Amico, Francesco Paolo

Publication type:

Article

Expanding the phenotype of 22q13.3 deletion: report of a case detected prenatally.

Published in:

Prenatal Diagnosis, 2008, v. 28, n. 10, p. 978, doi. 10.1002/pd.2110

By:

Maitz, Silvia;
Gentilin, Barbara;
Colli, Anna Maria;
Rizzuti, Tommaso;
Brandolisio, Emilia;
Vetro, Annalisa;
Zuffardi, Orsetta;
Guerneri, Silvana;
Lalatta, Faustina

Publication type:

Article

Norman-Roberts syndrome: characterization of the phenotype in early fetal life.

Published in:

Prenatal Diagnosis, 2007, v. 27, n. 6, p. 568, doi. 10.1002/pd.1728

By:

Natacci, Federica;
Bedeschi, Maria Francesca;
Righini, Andrea;
Inverardi, Francesca;
Rizzuti, Tommaso;
Boschetto, Chiara;
Triulzi, Fabio;
Spreafico, Roberto;
Frassoni, Carolina;
Lalatta, Faustina

Publication type:

Article

Limited value of echography to predict true fetal mosaicism for trisomy 12.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1186, doi. 10.1002/pd.1587

By:

Gentilin, Barbara;
Giardino, Daniela;
Boschetto, Chiara;
Guerneri, Silvana;
Fortuna, Renato;
Rizzuti, Tommaso;
Lalatta, Faustina

Publication type:

Article

Frontal bilateral megalencephaly: fetal and autopsy MR evaluation of an unclassified malformation.

Published in:

Prenatal Diagnosis, 2005, v. 25, n. 6, p. 489, doi. 10.1002/pd.1178

By:

Parazzini, Cecilia;
Righini, Andrea;
Lalatta, Faustina;
Bianchini, Elena;
Triulzi, Fabio

Publication type:

Article

Prenatal diagnosis of genetic syndromes may be facilitated by serendipitous findings at fetal blood sampling.

Published in:

Prenatal Diagnosis, 1998, v. 18, n. 8, p. 834, doi. 10.1002/(SICI)1097-0223(199808)18:8<834::AID-PD340>3.0.CO;2-6

By:

Lalatta, Faustina;
Salmona, Sarah;
Fogliani, Roberto;
Rizzuti, Tommaso;
Nicolini, Umberto

Publication type:

Article

Language Development in Sex Chromosome Trisomies: Developmental Profiles at 2 and 4 Years of Age, and Predictive Measures.

Published in:

Developmental Neurorehabilitation, 2022, v. 25, n. 5, p. 337, doi. 10.1080/17518423.2021.2020925

By:

Capelli, Elena;
Silibello, Gaia;
Ajmone, Paola Francesca;
Altamore, Elena;
Lalatta, Faustina;
Vizziello, Paola Giovanna;
Costantino, Maria Antonella;
Zampini, Laura

Publication type:

Article

Maternal input to children with sex chromosome trisomies.

Published in:

International Journal of Language & Communication Disorders (John Wiley & Sons, Inc.), 2020, v. 55, n. 5, p. 724, doi. 10.1111/1460-6984.12557

By:

Zampini, Laura;
Ferrante, Camilla;
Silibello, Gaia;
Dall'Ara, Francesca;
Rigamonti, Claudia;
Zanchi, Paola;
Vizziello, Paola Giovanna;
Lalatta, Faustina;
Costantino, Maria Antonella

Publication type:

Article

Vocal and gestural productions of 24‐month‐old children with sex chromosome trisomies.

Published in:

International Journal of Language & Communication Disorders (John Wiley & Sons, Inc.), 2018, v. 53, n. 1, p. 171, doi. 10.1111/1460-6984.12334

By:

Zampini, Laura;
Draghi, Lara;
Silibello, Gaia;
Dall'Ara, Francesca;
Rigamonti, Claudia;
Suttora, Chiara;
Zanchi, Paola;
Salerni, Nicoletta;
Lalatta, Faustina;
Vizziello, Paola

Publication type:

Article

Early communicative skills of children with Klinefelter syndrome.

Published in:

Clinical Linguistics & Phonetics, 2018, v. 32, n. 7, p. 577, doi. 10.1080/02699206.2017.1384853

By:

Zampini, Laura;
Burla, Tiziana;
Silibello, Gaia;
Dall’Ara, Francesca;
Rigamonti, Claudia;
Lalatta, Faustina;
Vizziello, Paola

Publication type:

Article

A novel missense mutation in ANO5/TMEM16E is causative for gnathodiaphyseal dyplasia in a large Italian pedigree.

Published in:

European Journal of Human Genetics, 2013, v. 21, n. 6, p. 613, doi. 10.1038/ejhg.2012.224

By:

Marconi, Caterina;
Brunamonti Binello, Paolo;
Badiali, Giovanni;
Caci, Emanuela;
Cusano, Roberto;
Garibaldi, Joseph;
Pippucci, Tommaso;
Merlini, Alberto;
Marchetti, Claudio;
Rhoden, Kerry J;
Galietta, Luis J V;
Lalatta, Faustina;
Balbi, Paolo;
Seri, Marco

Publication type:

Article

Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann syndrome.

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 5, p. 611, doi. 10.1038/ejhg.2008.233

By:

Bliek, Jet;
Verde, Gaetano;
Callaway, Jonathan;
Maas, Saskia M.;
De Crescenzo, Agostina;
Sparago, Angela;
Cerrato, Flavia;
Russo, Silvia;
Ferraiuolo, Serena;
Rinaldi, Maria Michela;
Fischetto, Rita;
Lalatta, Faustina;
Giordano, Lucio;
Ferrari, Paola;
Cubellis, Maria Vittoria;
Larizza, Lidia;
Temple, I. Karen;
Mannens, Marcel M. A. M.;
Mackay, Deborah J. G.;
Riccio, Andrea

Publication type:

Article

Beckwith–Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi.

Published in:

Epigenetics, 2015, v. 10, n. 7, p. 643, doi. 10.1080/15592294.2015.1057383

By:

Paganini, Leda;
Carlessi, Nicole;
Fontana, Laura;
Silipigni, Rosamaria;
Motta, Silvia;
Fiori, Stefano;
Guerneri, Silvana;
Lalatta, Faustina;
Cereda, Anna;
Sirchia, Silvia;
Miozzo, Monica;
Tabano, Silvia

Publication type:

Article

Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.

Published in:

Epigenetics, 2013, v. 8, n. 10, p. 1053, doi. 10.4161/epi.25812

By:

Calvello, Mariarosaria;
Tabano, Silvia;
Colapietro, Patrizia;
Maitz, Silvia;
Pansa, Alessandra;
Augello, Claudia;
Lalatta, Faustina;
Gentilin, Barbara;
Spreafico, Filippo;
Calzari, Luciano;
Perotti, Daniela;
Larizza, Lidia;
Russo, Silvia;
Selicorni, Angelo;
Sirchia, Silvia M.;
Miozzo, Monica

Publication type:

Article

Why women do not ask for information on preconception health? A qualitative study.

Published in:

2017

By:

Bortolus, Renata;
Oprandi, Nadia C.;
Morassutti, Francesca Rech;
Marchetto, Luca;
Filippini, Francesca;
Agricola, Eleonora;
Tozzi, Alberto E.;
Castellani, Carlo;
Lalatta, Faustina;
Rusticali, Bruno;
Mastroiacovo, Pierpaolo;
Rech Morassutti, Francesca

Publication type:

journal article

The introduction of QF-PCR in prenatal diagnosis of fetal aneuploidies: time for reconsideration.

Published in:

Human Reproduction Update, 2004, v. 10, n. 6, p. 541, doi. 10.1093/humupd/dmh046

By:

Umberto Nicolini;
Faustina Lalatta;
Federica Natacci;
Cristina Curcio;
The-Hung Bui

Publication type:

Article

Before Is Better: Innovative Multidisciplinary Preconception Care in Different Clinical Contexts.

Published in:

Journal of Clinical Medicine, 2023, v. 12, n. 19, p. 6352, doi. 10.3390/jcm12196352

By:

Cristodoro, Martina;
Dell'Avanzo, Marinella;
Ghio, Matilda;
Lalatta, Faustina;
Vena, Walter;
Lania, Andrea;
Sacchi, Laura;
Bravo, Maria;
Bulfoni, Alessandro;
Di Simone, Nicoletta;
Inversetti, Annalisa

Publication type:

Article

Web-Based Surveillance of Public Information Needs for Informing Preconception Interventions.

Published in:

PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0122551

By:

D’Ambrosio, Angelo;
Agricola, Eleonora;
Russo, Luisa;
Gesualdo, Francesco;
Pandolfi, Elisabetta;
Bortolus, Renata;
Castellani, Carlo;
Lalatta, Faustina;
Mastroiacovo, Pierpaolo;
Tozzi, Alberto Eugenio

Publication type:

Article

Daily life changes and adaptations investigated in 154 families with a child suffering from a rare disability at a public centre for rare diseases in Northern Italy.

Published in:

Italian Journal of Pediatrics, 2016, v. 42, p. 1, doi. 10.1186/s13052-016-0285-0

By:

Silibello, G.;
Vizziello, P.;
Gallucci, M.;
Selicorni, A.;
Milani, D.;
Ajmone, P. F.;
Rigamonti, C.;
De Stefano, S.;
Bedeschi, M. F.;
Lalatta, Faustina

Publication type:

Article

Language Development in the Second Year of Life: The Case of Children with Sex Chromosome Trisomies Diagnosed before Birth.

Published in:

International Journal of Environmental Research & Public Health, 2022, v. 19, n. 3, p. 1831, doi. 10.3390/ijerph19031831

By:

Zampini, Laura;
Lorini, Alessandra;
Silibello, Gaia;
Zanchi, Paola;
Dall'Ara, Francesca;
Ajmone, Paola Francesca;
Monti, Federico;
Lalatta, Faustina;
Costantino, Maria Antonella;
Vizziello, Paola Giovanna

Publication type:

Article

Increased RISK for 47,XXY on cell‐free DNA screen: Not always Klinefelter syndrome.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1255, doi. 10.1002/pd.5890

By:

Ronzoni, Luisa;
Bedeschi, Maria Francesca;
Silibello, Gaia;
Accurti, Veronica;
Di Segni, Marina;
Nicotra, Valeria;
Vizziello, Paola;
Lalatta, Faustina

Publication type:

Article

A comment on "clinical experience with sex chromosome aneuploidies detected by noninvasive prenatal testing (NIPT): Accuracy and patient decision-making".

Published in:

2018

By:

Ronzoni, Luisa;
Silibello, Gaia;
Quagliarini, Donatella;
Lalatta, Faustina

Publication type:

Letter

STAR syndrome plus: The first description of a female patient with the lethal form.

Published in:

American Journal of Medical Genetics. Part A, 2017, v. 173, n. 12, p. 3226, doi. 10.1002/ajmg.a.38484

By:

Bedeschi, Maria F.;
Giangiobbe, Sara;
Paganini, Leda;
Tabano, Silvia;
Silipigni, Rosamaria;
Colombo, Lorenzo;
Crippa, Beatrice L.;
Lalatta, Faustina;
Guerneri, Silvana;
Miozzo, Monica

Publication type:

Article

Prenatal Diagnosis of Simpson-Golabi-Behmel Syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2016, v. 170, n. 12, p. 3258, doi. 10.1002/ajmg.a.37873

By:

Magini, Pamela;
Palombo, Flavia;
Boito, Simona;
Lanzoni, Giulia;
Mongelli, Patrizia;
Rizzuti, Tommaso;
Baccarin, Marco;
Pippucci, Tommaso;
Seri, Marco;
Lalatta, Faustina

Publication type:

Article

Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: A genotype-phenotype analysis.

Published in:

American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 7, p. 1551, doi. 10.1002/ajmg.a.37063

By:

Ronzoni, Luisa;
Peron, Angela;
Bianchi, Vera;
Baccarin, Marco;
Guerneri, Silvana;
Silipigni, Rosamaria;
Lalatta, Faustina;
Bedeschi, Maria Francesca

Publication type:

Article

Response to 'Prenatal genetic counseling in klinefelter syndrome: Comments on the article by Lalatta and Tint [2013] and a proposal of a new approach' by Pimpolari et al.

Published in:

American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 3, p. 678, doi. 10.1002/ajmg.a.36892

By:

Lalatta, Faustina;
Tint, G Stephen

Publication type:

Article

Unusual prenatal presentation of Rubinstein-Taybi syndrome: A case report.

Published in:

American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 10, p. 2663, doi. 10.1002/ajmg.a.36684

By:

Bedeschi, Maria Francesca;
Crippa, Beatrice Letizia;
Colombo, Lorenzo;
Guez, Sophie;
Cerruti, Marta;
Fogliani, Roberto;
Gervasini, Cristina;
Lalatta, Faustina

Publication type:

Article

Counseling parents before prenatal diagnosis: Do we need to say more about the sex chromosome aneuploidies?

Published in:

American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 11, p. 2873, doi. 10.1002/ajmg.a.36226

By:

Lalatta, Faustina;
Tint, G Stephen

Publication type:

Article

Healthcare transition in patients with rare genetic disorders with and without developmental disability: Neurofibromatosis 1 and williams-beuren syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 7, p. 1666, doi. 10.1002/ajmg.a.35982

By:

Van Lierde, Andrea;
Menni, Francesca;
Bedeschi, Maria Francesca;
Natacci, Federica;
Guez, Sophie;
Vizziello, Paola;
Costantino, Maria Antonella;
Lalatta, Faustina;
Esposito, Susanna

Publication type:

Article

Prevalence of diabetes and pre-diabetes in a cohort of Italian young adults with Williams syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 4, p. 817, doi. 10.1002/ajmg.a.35655

By:

Masserini, Benedetta;
Bedeschi, Maria Francesca;
Bianchi, Vera;
Scuvera, Giulietta;
Beck‐Peccoz, Paolo;
Lalatta, Faustina;
Selicorni, Angelo;
Orsi, Emanuela

Publication type:

Article

Neurofibromatosis type 1 and pregnancy: Maternal complications and attitudes about prenatal diagnosis.

Published in:

American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 2, p. 386, doi. 10.1002/ajmg.a.35720

By:

Cesaretti, Claudia;
Melloni, Giulia;
Quagliarini, Donatella;
Fogliani, Roberto;
Zaina, Barbara;
Bedeschi, Maria Francesca;
Lalatta, Faustina;
Trespidi, Laura;
Natacci, Federica

Publication type:

Article