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1

Casa Satellite: Pilot Study for a Smart Home for People with Down Syndrome

Dalprà, Michela, Chiogna, M., Frattari, A., Primon, G.

Journal:

Journal of Architectural Engineering

Year:

2018

Language:

english

File:

PDF, 2.21 MB

english, 2018

2

Clinical and genetic evaluation of a family showing both autism and epilepsy

R. Combi, S. Redaelli, M. Beghi, M. Clerici, C.M. Cornaggia, L. Dalprà

Journal:

Brain Research Bulletin

Year:

2010

Language:

english

File:

PDF, 144 KB

english, 2010

3

Rearrangements and unstable chromosome lesions in epithelial ovarian cancer

L. Dalprà, G. Nocera, M.G. Tibiletti, M. Presti, F. Zanaboni

Journal:

Cancer Genetics and Cytogenetics

Year:

1989

Language:

english

File:

PDF, 69 KB

english, 1989

4

Genotype-phenotype correlation in two sets of monozygotic twins with Williams syndrome

Castorina, Pierangela, Selicorni, Angelo, Bedeschi, Francesca, Dalprà, Leda, Larizza, Lidia

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 263 KB

english, 1997

5

Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome

Monica Miozzo, Pierangela Castorina, Paola Riva, Leda Dalprà, Anna Maria Fuhrman Conti, Ludovica Volpi, Tuck S. Hoe, Alan Khoo, Joop Wiegant, Carla Rosenberg, Lidia Larizza

Journal:

International Journal of Cancer

Year:

1998

Language:

english

File:

PDF, 383 KB

english, 1998

6

First cytogenetic study of a recurrent familial chordoma of the clivus

Leda Dalprà, Roberta Malgara, Monica Miozzo, Paola Riva, Marinella Volonté, Lidia Larizza, Anna M. Fuhrman Conti

Journal:

International Journal of Cancer

Year:

1999

Language:

english

File:

PDF, 895 KB

english, 1999

7

A tumor suppressor locus in familial and sporadic chordoma maps to 1p36

Monica Miozzo, Leda Dalprà, Paola Riva, Marinella Volontà, Fabio Macciardi, Sergio Pericotti, M. Grazia Tibiletti, Michele Cerati, Klaus Rohde, Lidia Larizza, A. Maria Fuhrman Conti

Journal:

International Journal of Cancer

Year:

2000

Language:

english

File:

PDF, 150 KB

english, 2000

8

A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency

Rosanna Pallotta, Leda Dalprà, Monica Miozzo, Tamara Ehresmann, Paola Fusilli

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 132 KB

english, 2001

9

Fetal trisomy 5 mosaicism: Case report and literature review

Nicoletta Villa, Serena Redaelli, Cesarina Borroni, Carla Colombo, Nadia Roncaglia, Elena Sala, Francesca Crosti, Anna Cappellini, Leda Dalprà

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 76 KB

english, 2007

10

A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome

Emanuela Martinoli, Gian Vincenzo Zuccotti, Laura Pogliani, Marinella Volontè, Marco Venturin, Paolo Fortina, Adam Ertel, Serena Redaelli, Paola Riva, Leda Dalprà

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 127 KB

english, 2010

11

A de novo supernumerary genomic discontinuous ring chromosome 21 in a child with mild intellectual disability

Nicoletta Villa, Angela Bentivegna, Adam Ertel, Serena Redaelli, Carla Colombo, Renata Nacinovich, Fiorenza Broggi, Sara Lissoni, Silvia Bungaro, Sankar Addya, Paolo Fortina, Leda Dalprà

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 266 KB

english, 2011

12

Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene

Romina Combi, Leda Dalprà, Luigi Ferini-Strambi, Maria L. Tenchini

Journal:

Annals of Neurology

Year:

2005

Language:

english

File:

PDF, 185 KB

english, 2005

13

A balanced chromosomal translocation disrupting ARHGEF9 is associated with epilepsy, anxiety, aggression, and mental retardation

Vera M. Kalscheuer, Luciana Musante, Cheng Fang, Kirsten Hoffmann, Celine Fuchs, Eloisa Carta, Emma Deas, Kanamarlapudi Venkateswarlu, Corinna Menzel, Reinhard Ullmann, Niels Tommerup, Leda Dalprà, An

Journal:

Year:

2009

Language:

english

File:

PDF, 1.12 MB

english, 2009

14

A rescuable folding defective Nav1.1 (SCN1A) sodium channel mutant causes GEFS+: Common mechanism in Nav1.1 related epilepsies?

Raffaella Rusconi, Romina Combi, Sandrine Cestèle, Daniele Grioni, Silvana Franceschetti, Leda Dalprà, Massimo Mantegazza

Journal:

Year:

2009

Language:

english

File:

PDF, 822 KB

english, 2009

15

Mapping of candidate region for chordoma development to 1p36.13 by LOH analysis

Paola Riva, Francesca Crosti, Francesca Orzan, Leda Dalprà, Pietro Mortini, Antonina Parafioriti, Bianca Pollo, Anna Maria Fuhrman Conti, Monica Miozzo, Lidia Larizza

Journal:

International Journal of Cancer

Year:

2003

Language:

english

File:

PDF, 209 KB

english, 2003

16

Mutational Analysis of Nicotinic Acetylcholine Receptor β2 Subunit Gene (CHRNB2) in a Representative Cohort of Italian Probands Affected by Autosomal Dominant Nocturnal Frontal Lobe Epilepsy

Stefano Duga, Rosanna Asselta, Maria Teresa Bonati, Massimo Malcovati, Leda Dalprà, Alessandro Oldani, Marco Zucconi, Luigi Ferini-Strambi, Maria Luisa Tenchini

Journal:

Year:

2002

Language:

english

File:

PDF, 42 KB

english, 2002

17

Do parent's global rating of well-being and disease activity of children with juvenile idiopathic arthritis yield different information?

N Ullmann, A Consolaro, G Filocamo, S Verazza, S Dalprà, C Ferrari, R Caorsi, S Viola, C Visconti, A Martini, A Ravelli

Journal:

Pediatric Rheumatology

Year:

2008

Language:

english

File:

PDF, 73 KB

english, 2008

18

Comparison of physician's, parent's and patient's global ratings made on linear or 21-circle visual analogue scales (VAS) in juvenile idiopathic arthritis (JIA)

S Dalprà, S Verazza, C Ferrari, A Parodi, S Davì, B Schiappapietra, A Consolaro, G Filocamo, S Viola, A Martini, A Ravelli

Journal:

Pediatric Rheumatology

Year:

2008

Language:

english

File:

PDF, 96 KB

english, 2008

19

Etanercept efficacy in the treatment of chronic isolated inflammatory coxitis

A Parodi, P Picco, C Malattia, S Davì, S Dalprà, F Traverso, MC Ponti, A Buoncompagni, A Loy, S Viola, A Martini

Journal:

Pediatric Rheumatology

Year:

2008

Language:

english

File:

PDF, 64 KB

english, 2008

20

Time of onset of iridocyclitis (IC) in children with juvenile idiopathic arthritis (JIA)

S Verazza, M Allegra, B Lattanzi, S Dalprà, S Magni-Manzoni, A Pistorio, S Oliveira, E Castell, O Arguedas, A Martini, A Ravelli

Journal:

Pediatric Rheumatology

Year:

2008

Language:

english

File:

PDF, 233 KB

english, 2008

21

Children with juvenile idiopathic arthritis currently followed in a tertiary care setting have a better psychosocial well-being than healthy peers

M Bertamino, A Consolaro, B Lattanzi, S Magni-Manzoni, S Lanni, C Suffia, S Dalprà, S Rosina, A Martini, A Ravelli

Journal:

Pediatric Rheumatology

Year:

2011

Language:

english

File:

PDF, 174 KB

english, 2011

22

Chromosome territories, X;Y translocation and Premature Ovarian Failure: is there a relationship?

Sara Lissoni, Simona Baronchelli, Nicoletta Villa, Valeria Lucchini, Enrico Betri, Pietro Cavalli, Leda Dalprà

Journal:

Molecular Cytogenetics

Year:

2009

Language:

english

File:

PDF, 1.04 MB

english, 2009

23

Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism: a case report and review of literature

Serena Redaelli, Elena Sala, Nadia Roncaglia, Carla Colombo, Francesca Crosti, Nicoletta Villa, Paolo Tagliabue, Anna Cappellini, Leda Dalprà

Journal:

Prenatal Diagnosis

Year:

2005

Language:

english

File:

PDF, 238 KB

english, 2005

24

Routine chromosome analysis on fetal blood microaliquots obtained at fetoscopy

G. Simoni, M. G. Tibiletti, L. Dalprà, M. Ferrari, B. Brambati

Journal:

Prenatal Diagnosis

Year:

1983

Language:

english

File:

PDF, 380 KB

english, 1983

25

A rare non-heterochromatic 9p+ variant in two amniotic fluid cell cultures

N. Archidiacono, V. Pecile, M. Rocchi, L. Dalpra, G. Nocera, G. Simoni

Journal:

Prenatal Diagnosis

Year:

1984

Language:

english

File:

PDF, 145 KB

english, 1984

26

Five cases of prenatally diagnosed sex chromosome mosaicism

G. Nocera, L. Dalpra, M. G. Tibiletti, M. Buscglia

Journal:

Prenatal Diagnosis

Year:

1985

Language:

english

File:

PDF, 432 KB

english, 1985

27

The use of amniotic FSH levels in resolving a discrepancy between fetal chromosomal and phenotypic sex

L. Dalprà, M. Castagni, G. Nocera, M. G. Tibiletti, G. Riboni, S. Agosti

Journal:

Prenatal Diagnosis

Year:

1985

Language:

english

File:

PDF, 304 KB

english, 1985

28

‘Late’ chorionic villus sampling: Cytogenetic aspects

L. Dalprà, G. Nocera, M. G. Tibiletti, E. Martinoli, A. Oldrini, S. Agosti, P. G. Crosignani

Journal:

Prenatal Diagnosis

Year:

1993

Language:

english

File:

PDF, 377 KB

english, 1993

29

Transverse limb reduction defects after chorion villus sampling: A retrospective Cohort study

Professor Pierpaolo Mastroiacovo, Alberto Eugenio Tozzi, Silvano Agosti, Giancarlo Bocchino, Luciano Bovicelli, Leda Dalprà, Laura Doria Laba Carbone, Mario Lituania, Angelica Luttichau, Franco Manteg

Journal:

Prenatal Diagnosis

Year:

1993

Language:

english

File:

PDF, 380 KB

english, 1993

30

The predictive value of cytogenetic diagnosis after CVS based on 4860 cases with both direct and culture methods

Dr M. C. Pittalis, L. Dalprà, F. Torricelli, N. Rizzo, G. Nocera, E. Cariati, L. Santarini, M. G. Tibiletti, S. Agosti, L. Bovicelli, A. Forabosco

Journal:

Prenatal Diagnosis

Year:

1994

Language:

english

File:

PDF, 882 KB

english, 1994

31

Identification of a small supernumerary marker chromosome, r(2)(p10q11.2), and the problem of determining prognosis

N. Villa, P. Riva, D. Colombo, E. Sala, S. Mariani, C. Zorloni, F. Crosti, L. Dalprà

Journal:

Prenatal Diagnosis

Year:

2001

Language:

english

File:

PDF, 160 KB

english, 2001

32

Floristic changes in the River Tees

B. A. Whitton, M. Dalpra

Journal:

Year:

1968

Language:

english

File:

PDF, 309 KB

english, 1968

33

Satellite associations and silver staining in a case of multiple G and D variants

R. Lernia, M. L. Riva, L. Dalprà, E. Ginelli

Journal:

Year:

1980

Language:

english

File:

PDF, 665 KB

english, 1980

34

A duplication-deficiency X chromosome in a girl with severe mental retardation

N. Sacchi, L. Dalprà, E. Kehyayan

Journal:

Year:

1980

Language:

english

File:

PDF, 506 KB

english, 1980

35

Differences in the levels of UV repair and in clinical symptoms in two sibs affected by xeroderma pigmentosum

Miria Stefanini, Wilma Keijzer, Leda Dalprà, Raffaella Elli, Marcella Nazzaro Porro, B. Nicoletti, Fiorella Nuzzo

Journal:

Year:

1980

Language:

english

File:

PDF, 619 KB

english, 1980

36

Cytogenetic findings in 4952 prenatal diagnoses. An Italian collaborative study

G. Simoni, M. Fraccaro, A. Arslanian, M. Bacchetta, C. Baccichetti, F. A. Bignone, A. Cagiano, A. O. Carbonara, F. Carozzi, C. Cuoco, F. Dagna Bricarelli, B. Dallapiccola, L. Dalprà, L. Doria Lamba Ca

Journal:

Year:

1982

Language:

english

File:

PDF, 484 KB

english, 1982

37

Ring chromosome 10 Associated with multiple congenital malformations

G. Simoni, F. Rossella, L. Dalprà, G. Visconti, C. Piria-Schwarz

Journal:

Year:

1979

Language:

english

File:

PDF, 435 KB

english, 1979

38

The offspring of marriage between two first cousins with the same reciprocal translocation t(2;7)(p11;q31)

G. Simoni, L. Dalprà, G. L. Terzoli, F. Rossella, M. G. Tibiletti

Journal:

Year:

1980

Language:

english

File:

PDF, 324 KB

english, 1980

39

A woman carrier of two apparently unrelated reciprocal translocations

G. Simoni, E. Montali, F. Rossella, L. Dalprà, F. Curto

Journal:

Year:

1979

Language:

english

File:

PDF, 176 KB

english, 1979

40

The 11q;22q translocation: A collaborative study of 20 new cases and analysis of 110 families

L. Iselius, J. Lindsten, A. Aurias, M. Fraccaro, C. Bastard, A. M. Bottelli, T. -H. Bui, D. Caufin, L. Dalprà, N. Delendi, B. Dutrillaux, Y. Fukushima, J. P. M. Geraedts, J. Grouchy, J. Gyftodimou, A.

Journal:

Year:

1983

Language:

english

File:

PDF, 2.99 MB

english, 1983

41

Expression of three rare fragile sites: chromosomal truncation, amplification of distal segment and telomeric renewal

N. Villa, L. Dalprà, L. Larizza

Journal:

Year:

1997

Language:

english

File:

PDF, 583 KB

english, 1997

42

Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated families

Maria Teresa Bonati, Romina Combi, Rosanna Asselta, Stefano Duga, Massimo Malcovati, Alessandro Oldani, Marco Zucconi, Luigi Ferini-Strambi, Leda Dalprà, Maria Luisa Tenchini

Journal:

Journal of Neurology

Year:

2002

Language:

english

File:

PDF, 935 KB

english, 2002

43

Autosomal dominant nocturnal frontal lobe epilepsy

R. Combi, L. Dalprà, M. L. Tenchini, Luigi Ferini-Strambi

Journal:

Journal of Neurology

Year:

2004

Language:

english

File:

PDF, 471 KB

english, 2004

44

Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure

Anna Marozzi, Emanuela Manfredini, Maria Tibiletti, Daniela Furlan, Nicoletta Villa, Walter Vegetti, Pier Crosignani, Enrico Ginelli, Raffaella Meneveri, Leda Dalprà

Journal:

Year:

2000

Language:

english

File:

PDF, 157 KB

english, 2000

45

Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome

Paola Riva, Pierangela Castorina, Siranoush Manoukian, Leda Dalprà, Luisa Doneda, Giuseppe Marini, Johannes den Dunnen, L. Larizza

Journal:

Year:

1996

Language:

english

File:

PDF, 346 KB

english, 1996

46

E. colivirulence factors in children with neurogenic bladder associated with bacteriuria

Eliana B. M. Guidoni, Vanessa A. Dalpra, Patrícia Maria Figueiredo, Domingos da Silva Leite, Lycia Mara J. Mímica, Tomomasa Yano, Jesus E. Blanco, Julio Toporovski

Journal:

Pediatric Nephrology

Year:

2006

Language:

english

File:

PDF, 157 KB

english, 2006

47

Characterisation of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams–Beuren syndrome region in chromosomal rearrangements

Giorgio Portera, Marco Venturin, Antonella Patrizi, Emanuela Martinoli, Paola Riva, Leda Dalprà

Journal:

Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 468 KB

english, 2006

48

Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptorCHRNA5/A3/B4gene cluster and identification of novel intragenic polymorphisms

S. Duga, G. Soldà, R. Asselta, M. T. Bonati, L. Dalprà, M. Malcovati, M. L. Tenchini

Journal:

Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 443 KB

english, 2001

49

Decreased platelet glutamate uptake and genetic risk factors in patients with Parkinson's disease

C. Ferrarese, L. Tremolizzo, M. Rigoldi, G. Sala, B. Begni, L. Brighina, G. Ricci, M. G. Albizzati, R. Piolti, F. Crosti, L. Dalprà, L. Frattola

Journal:

Neurological Sciences

Year:

2001

Language:

english

File:

PDF, 43 KB

english, 2001

50

Monitoring the genomic stability of in vitro cultured rat bone-marrow-derived mesenchymal stem cells

Dana Foudah, Serena Redaelli, Elisabetta Donzelli, Angela Bentivegna, Mariarosaria Miloso, Leda Dalprà, Giovanni Tredici

Journal:

Chromosome Research

Year:

2009

Language:

english

File:

PDF, 663 KB

english, 2009

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