G. Concolino: search on Z-Library

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1

Uno specchio infranto. Adolescenti e abuso sessuale nell’opera di Alberto Moravia

Abram, Bianca Concolino Mancini

Journal:

Italian Studies

Year:

2016

Language:

italian

File:

PDF, 332 KB

italian, 2016

2

Cow’s Milk Protein Allergy in Infancy: A Risk Factor for Functional Gastrointestinal Disorders in Children?

Pensabene, Licia, Salvatore, Silvia, D'Auria, Enza, Parisi, Francesca, Concolino, Daniela, Borrelli, Osvaldo, Thapar, Nikhil, Staiano, Annamaria, Vandenplas, Yvan, Saps, Miguel

Journal:

Year:

2018

Language:

english

File:

PDF, 475 KB

english, 2018

3

New Strategies for the Treatment of Phenylketonuria (PKU)

Strisciuglio, Pietro, Concolino, Daniela

Journal:

Year:

2014

Language:

english

File:

PDF, 240 KB

english, 2014

4

Integration of “Omics” Strategies for Biomarkers Discovery and for the Elucidation of Molecular Mechanisms Underlying Brugada Syndrome

Scumaci, Domenica, Oliva, Antonio, Concolino, Antonio, Curcio, Antonio, Fiumara, Claudia Vincenza, Tammè, Laura, Campuzano, Oscar, Pascali, Vincenzo L., Coll, Monica, Iglesias, Anna, Berne, Paola, Cas

Journal:

PROTEOMICS - Clinical Applications

Year:

2018

Language:

english

File:

PDF, 1.54 MB

english, 2018

5

The Legal Framework of the “War On Terrorism”

Barbara Concolino

Journal:

Criminal Law Forum

Year:

2008

Language:

english

File:

PDF, 132 KB

english, 2008

6

Multiplex ligation-dependent probe amplification (MLPA) assay for the detection of CYP21A2 gene deletions/duplications in Congenital Adrenal Hyperplasia: First technical report

Paola Concolino, Enrica Mello, Vincenzo Toscano, Franco Ameglio, Cecilia Zuppi, Ettore Capoluongo

Journal:

Clinica Chimica Acta

Year:

2009

Language:

english

File:

PDF, 693 KB

english, 2009

7

Redefining the Pulvinar Sign in Fabry Disease

Cocozza, S., Russo, C., Pisani, A., Olivo, G., Riccio, E., Cervo, A., Pontillo, G., Feriozzi, S., Veroux, M., Battaglia, Y., Concolino, D., Pieruzzi, F., Mignani, R., Borrelli, P., Imbriaco, M., Brune

Journal:

American Journal of Neuroradiology

Year:

2017

Language:

english

File:

PDF, 816 KB

english, 2017

8

Clinical efficacy of Enzyme Replacement Therapy in paediatric Hunter patients, an independent study of 3.5 years

Tomanin, Rosella, Zanetti, Alessandra, D’Avanzo, Francesca, Rampazzo, Angelica, Gasparotto, Nicoletta, Parini, Rossella, Pascarella, Antonia, Concolino, Daniela, Procopio, Elena, Fiumara, Agata, Borgo

Journal:

Orphanet Journal of Rare Diseases

Year:

2014

Language:

english

File:

PDF, 689 KB

english, 2014

9

Congenital hypertrichosis, cardiomegaly, and osteochondrodysplasia (Cant� syndrome): A new case with unusual radiological findings

Concolino, D., Formicola, S., Camera, G., Strisciuglio, P.

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 274 KB

english, 2000

10

Facial Dysmorphisms, Macrodontia, Focal Epilepsy, and Thinning of the Corpus Callosum: A Rare Mild Form of Kabuki Syndrome

Bruni, Valentina, Scozzafava, Cristina, Gnazzo, Maria, Parisi, Francesca, Sestito, Simona, Pensabene, Licia, Novelli, Antonio, Concolino, Daniela

Journal:

Journal of Pediatric Genetics

Year:

2020

File:

PDF, 1.18 MB

2020

11

Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations

Concolino, Paola, Mello, Enrica, Zuppi, Cecilia, Capoluongo, Ettore

Journal:

Clinical Chemistry and Laboratory Medicine

Year:

2010

Language:

english

File:

PDF, 136 KB

english, 2010

12

Long-term follow-up of patients with phenylketonuria treated with tetrahydrobiopterin: a seven years experience

Scala, Iris, Concolino, Daniela, Casa, Roberto, Nastasi, Anna, Ungaro, Carla, Paladino, Serena, Capaldo, Brunella, Ruoppolo, Margherita, Daniele, Aurora, Bonapace, Giuseppe, Strisciuglio, Pietro, Pare

Journal:

Orphanet Journal of Rare Diseases

Year:

2015

Language:

english

File:

PDF, 521 KB

english, 2015

13

Reactions of Tetrakis(dimethylamide)−Titanium, −Zirconium and −Hafnium with Silanes: Synthesis of Unusual Amide Hydride Complexes and Mechanistic Studies of Titanium−Silicon−Nitride (Ti−Si−N) Formation

Liu, Xiaozhan, Wu, Zhongzhi, Cai, Hu, Yang, Yihui, Chen, Tianniu, Vallet, Catherine E., Zuhr, Ray A., Beach, David B., Peng, Zhi-Hui, Wu, Yun-Dong, Concolino, Thomas E., Rheingold, Arnold L., Xue, Zil

Journal:

Journal of the American Chemical Society

Year:

2001

Language:

english

File:

PDF, 174 KB

english, 2001

14

Pathobiological Insights into Neurological Involvement in Cobalamin C Deficiency

Ceravolo, Ferdinando, Grisolia, Michele, Nicolettti, Angela, Sestito, Simona, Salpietro, Vincenzo, Polizzi, Agata, Ruggieri, Martino, Bonapace, Giuseppe, Pascale, Elisa, Concolino, Daniela

Journal:

Journal of Pediatric Biochemistry

Year:

2016

Language:

english

File:

PDF, 132 KB

english, 2016

15

The Different Forms of Mucopolysaccharidosis with Neurological Involvement: A Case-Based Review

Falvo, Francesca, Sestito, Simona, Nicoletti, Angela, Grisolia, Michele, Mascaro, Italia, Pascale, Elisa, Salpietro, Vincenzo, Polizzi, Agata, Ruggieri, Martino, Concolino, Daniela

Journal:

Journal of Pediatric Biochemistry

Year:

2016

Language:

english

File:

PDF, 287 KB

english, 2016

16

A comprehensive BRCA1/2 NGS pipeline for an immediate Copy Number Variation (CNV) detection in breast and ovarian cancer molecular diagnosis

Concolino, Paola, Rizza, Roberta, Mignone, Flavio, Costella, Alessandra, Guarino, Donatella, Carboni, Ilaria, Capoluongo, Ettore, Santonocito, Concetta, Urbani, Andrea, Minucci, Angelo

Journal:

Clinica Chimica Acta

Year:

2018

Language:

english

File:

PDF, 2.55 MB

english, 2018

17

Linkage between I172N mutation, a marker of 21-hydroxylase deficiency, and a single nucleotide polymorphism in Int6 of CYP21B gene: A genetic study of Sardinian family

Paola Concolino, Maria Antonia Satta, Concetta Santonocito, Cinzia Carrozza, Sandro Rocchetti, Franco Ameglio, Emiliano Giardina, Cecilia Zuppi, Ettore Capoluongo

Journal:

Clinica Chimica Acta

Year:

2006

Language:

english

File:

PDF, 246 KB

english, 2006

18

Fighting Terrorism, Respecting Human Rights

Barbara Concolino

Journal:

Criminal Law Forum

Year:

2007

Language:

english

File:

PDF, 135 KB

english, 2007

19

Postinfectious Functional Gastrointestinal Disorders in Children: A Multicenter Prospective Study

Pensabene, Licia, Talarico, Valentina, Concolino, Daniela, Ciliberto, Domenico, Campanozzi, Angelo, Gentile, Teresa, Rutigliano, Vincenzo, Salvatore, Silvia, Staiano, Annamaria, Di Lorenzo, Carlo

Journal:

The Journal of Pediatrics

Year:

2015

Language:

english

File:

PDF, 413 KB

english, 2015

20

Ecological Degradation: Pirandello’s Natural World in Paolo and Vittorio Taviani’s Kaos

Concolino, Christopher F.

Journal:

Italian Culture

Year:

2016

Language:

english

File:

PDF, 396 KB

english, 2016

21

Mind the gut: probiotics in paediatric neurogastroenterology

Salvatore, S., Pensabene, L., Borrelli, O., Saps, M., Thapar, N., Concolino, D., Staiano, A., Vandenplas, Y.

Journal:

Beneficial Microbes

Year:

2018

Language:

english

File:

PDF, 386 KB

english, 2018

22

Functional and morphological cardiovascular alterations associated with neurofibromatosis 1

CutruzzolÃ , Antonio, Irace, Concetta, Frazzetto, Marco, Sabatino, Jolanda, Gullace, Rosa, De Rosa, Salvatore, Spaccarotella, Carmen, Concolino, Daniela, Indolfi, Ciro, Gnasso, Agostino

Journal:

Scientific Reports

Year:

2020

File:

PDF, 1.11 MB

2020

23

Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy

Parini, Rossella, De Lorenzo, Paola, Dardis, Andrea, Burlina, Alberto, Cassio, Alessandra, Cavarzere, Paolo, Concolino, Daniela, Della Casa, Roberto, Deodato, Federica, Donati, Maria Alice, Fiumara, A

Journal:

Orphanet Journal of Rare Diseases

Year:

2018

Language:

english

File:

PDF, 699 KB

english, 2018

24

Centric fission of chromosome 9 in a boy with trisomy 9p

Concolino, D., Cinti, R., Moricca, M., Andria, G., Strisciuglio, P.

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 142 KB

english, 1998

25

W2(μ-H)2Cl4(μ-dppm)2: the bulk synthesis of a bridging hydride

Thomas E. Concolino, Judith L. Eglin, Edward J. Valente, Jeffrey D. Zubkowski

Journal:

Year:

1997

Language:

english

File:

PDF, 377 KB

english, 1997

26

Long-term treatment with recombinant insulin-like growth factor 1 (IGF-1) in a child withIGF-1gene mutation

Daniela Concolino, Gianluca Muzzi, Simona Sestito, Giovanna Vega, Giuseppe Bonapace, Pietro Strisciuglio

Journal:

European Journal of Pediatrics

Year:

2010

Language:

english

File:

PDF, 92 KB

english, 2010

27

Steroid receptors in metastases froh human renal cell carcinoma (RCC)

G. Concolino, E. Petrangeli, C. Panfili, R. Tenaglia, F. Di Silverio

Journal:

Journal of Steroid Biochemistry

Year:

1986

Language:

english

File:

PDF, 165 KB

english, 1986

28

High Resolution Melting Analysis (HRMA) for the identification of a rare UGT1A1 promoter polymorphism

Angelo Minucci, Enrica Mello, Domenico Tripodi, Paola Concolino, Cecilia Zuppi, Ettore Capoluongo

Journal:

Clinical Biochemistry

Year:

2011

Language:

english

File:

PDF, 395 KB

english, 2011

29

GAPO syndrome associated with vestibular dysfunction and hearing loss

Rapsomaniki, M., Chiarella, G., Mascaro, I., Ceravolo, F., Cassandro, E., Strisciuglio, P., Concolino, D.

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 78 KB

english, 2013

30

Home infusion program with enzyme replacement therapy for Fabry disease: The experience of a large Italian collaborative group

Concolino, D., Amico, L., Cappellini, M.D., Cassinerio, E., Conti, M., Donati, M.A., Falvo, F., Fiumara, A., Maccarone, M., Manna, R., Matucci, A., Musumeci, M.B., Nicoletti, A., Nisticò, R., Papadia,

Journal:

Molecular Genetics and Metabolism Reports

Year:

2017

Language:

english

File:

PDF, 181 KB

english, 2017

31

High-resolution melting analysis coupled with next-generation sequencing as a simple tool for the identification of a novel somatic BRCA2 variant: a case report

Costella, Alessandra, De Leo, Rossella, Guarino, Donatella, D’Indinosante, Marco, Concolino, Paola, Mazzuccato, Giorgia, Urbani, Andrea, Scambia, Giovanni, Capoluongo, Ettore, Fagotti, Anna, Minucci,

Journal:

Human Genome Variation

Year:

2018

Language:

english

File:

PDF, 956 KB

english, 2018

32

Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathy

Giovanni Cuda, Andrea Mussari, Daniela Concolino, Francesco S. Costanzo, Pietro Strisciuglio

Journal:

Year:

2002

Language:

english

File:

PDF, 208 KB

english, 2002

33

Slight association between type 1 diabetes and “ff” VDR FokI genotype in patients from the Italian Lazio Region. Lack of association with diabetes complications

E. Capoluongo, D. Pitocco, P. Concolino, C. Santonocito, E. Di Stasio, G. d'Onofrio, A. Manto, B. Giardina, G. Ghirlanda, F. Ameglio, Cecilia Zuppi

Journal:

Clinical Biochemistry

Year:

2006

Language:

english

File:

PDF, 122 KB

english, 2006

34

[Mn18]2+ and [Mn21]4+ single-molecule magnets

E.C. Sañudo, E.K. Brechin, C. Boskovic, W. Wernsdorfer, J. Yoo, A. Yamaguchi, T.R. Concolino, K.A. Abboud, A.L. Rheingold, H. Ishimoto, D.N. Hendrickson, G. Christou

Journal:

Year:

2003

Language:

english

File:

PDF, 469 KB

english, 2003

35

Ploidy and steroid receptors (SR) in human renal cell carcinoma (RCC)

G. Concolino, E. Petrangeli, R. Tenaglia, R. De Vita, C. Conti, E Di Silverio

Journal:

Journal of Steroid Biochemistry

Year:

1987

Language:

english

File:

PDF, 142 KB

english, 1987

36

Electroclinical evolution in ring chromosome 20 epilepsy syndrome: A case with severe phenotypic features followed for 25 years

F.A. de Falco, P. Olivieri, A. de Falco, D. Concolino, F. Battaglia, R. Verardi, G. Grande, M. Stabile

Journal:

Year:

2006

Language:

english

File:

PDF, 353 KB

english, 2006

37

17β-Hydroxysteroid dehydrogenase-3 deficiency: From pregnancy to adolescence

Bertelloni, S., Balsamo, A., Giordani, L., Fischetto, R., Russo, G., Delvecchio, M., Gennari, M., Nicoletti, A., Maggio, M. C., Concolino, D., Cavallo, L., Cicognani, A., Chiumello, G., Hiort, O., Bar

Journal:

Journal of Endocrinological Investigation

Year:

2009

Language:

english

File:

PDF, 97 KB

english, 2009

38

Differentiated Thyroid Cancer in Two Patients with Resistance to Thyroid Hormone

Paragliola, Rosa Maria, Lovicu, Rosa Maria, Locantore, Pietro, Senes, Paola, Concolino, Paola, Capoluongo, Ettore, Pontecorvi, Alfredo, Corsello, Salvatore Maria

Journal:

Year:

2011

Language:

english

File:

PDF, 113 KB

english, 2011

39

Successful management of neonatal renal venous thrombosis

Piscitelli, Antonio, Galiano, Rossella, Piccolo, Vincenzo, Concolino, Daniela, Strisciuglio, Pietro

Journal:

Pediatrics International

Year:

2014

Language:

english

File:

PDF, 215 KB

english, 2014

40

Urine Bikunin as a Marker of Renal Impairment in Fabry's Disease

Lepedda, Antonio Junior, Fancellu, Laura, Zinellu, Elisabetta, De Muro, Pierina, Nieddu, Gabriele, Deiana, Giovanni Andrea, Canu, Piera, Concolino, Daniela, Sestito, Simona, Formato, Marilena, Sechi,

Journal:

BioMed Research International

Year:

2013

Language:

english

File:

PDF, 1.45 MB

english, 2013

41

Early diagnosis of mucopolysaccharidoses in developing countries: A low cost and easy execution approach

Gabrielli, Orazio, Zampini, Lucia, Monachesi, Chiara, Marchesiello, Rita Lucia, Padella, Lucia, Santoro, Lucia, Volpi, Nicola, Concolino, Daniela, Fiumara, Agata, Rigon, Laura, Mazzoli, Milena, Carnie

Journal:

Clinica Chimica Acta

Year:

2017

Language:

english

File:

PDF, 270 KB

english, 2017

42

Composition and structure of glycosaminoglycans in DBS from 2-3-day-old newborns for the diagnosis of mucopolysaccharidosis

Maccari, Francesca, Galeotti, Fabio, Mantovani, Veronica, Zampini, Lucia, Padella, Lucia, Rigon, Laura, Concolino, Daniela, Fiumara, Agata, Pascale, Elisa, Pittalà, Annarita, Galeazzi, Tiziana, Monach

Journal:

Analytical Biochemistry

Year:

2018

Language:

english

File:

PDF, 686 KB

english, 2018

43

Low FODMAPs diet for functional abdominal pain disorders in children: critical review of current knowledge

Pensabene, Licia, Salvatore, Silvia, Turco, Rossella, Tarsitano, Flora, Concolino, Daniela, Baldassarre, Maria Elisabetta, Borrelli, Osvaldo, Thapar, Nikhil, Vandenplas, Yvan, Staiano, Annamaria, Saps

Journal:

Jornal de Pediatria

Year:

2019

Language:

english

File:

PDF, 1012 KB

english, 2019

44

Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by fragile X tremor ataxia syndrome

Bonapace, Giuseppe, Gullace, Rosa, Concolino, Daniela, Iannello, Grazia, Procopio, Radha, Gagliardi, Monica, Arabia, Gennarina, Barbagallo, Gaetano, Lupo, Angela, Manfredini, Lucia Ilaria, Annesi, Gra

Journal:

Year:

2019

Language:

english

File:

PDF, 1007 KB

english, 2019

45

Renal Cancer Steroid Receptors: Biochemical Basis for Endocrine Therapy

Concolino, G., Di Silverio, F., Marocchi, A., Bracci, U.

Journal:

European Urology

Year:

1979

File:

PDF, 371 KB

1979

46

Description of a novel missense mutation of glucose-6-phosphate dehydrogenase gene associated with asymptomatic high enzyme deficiency

Angelo Minucci, Paola Concolino, Mirca Antenucci, Concetta Santonocito, Franco Ameglio, Cecilia Zuppi, Bruno Giardina, Ettore Capoluongo

Journal:

Clinical Biochemistry

Year:

2007

Language:

english

File:

PDF, 244 KB

english, 2007

47

Brain and spine MRI features of Hunter disease: frequency, natural evolution and response to therapy

Renzo Manara, Elena Priante, Marco Grimaldi, Lucia Santoro, Luca Astarita, Rita Barone, Daniela Concolino, Maja Di Rocco, Maria Alice Donati, Simona Fecarotta, Anna Ficcadenti, Agata Fiumara, Francesc

Journal:

Journal of Inherited Metabolic Disease

Year:

2011

Language:

english

File:

PDF, 859 KB

english, 2011

48

Phenotypic variability, neurological outcome and genetics background of 6-pyruvoyl-tetrahydropterin synthase deficiency

V Leuzzi, Ca Carducci, Cl Carducci, S Pozzessere, A Burlina, R Cerone, D Concolino, MA Donati, L Fiori, C Meli, A Ponzone, F Porta, P Strisciuglio, I Antonozzi, N Blau

Journal:

Clinical Genetics

Year:

2010

Language:

english

File:

PDF, 516 KB

english, 2010

49

GSTM1-null polymorphism as possible risk marker for hypertension: Results from the aging and longevity study in the Sirente Geographic Area (ilSIRENTE study)

Ettore Capoluongo, Graziano Onder, Paola Concolino, Andrea Russo, Concetta Santonocito, Roberto Bernabei, Cecilia Zuppi, Franco Ameglio, Francesco Landi

Journal:

Clinica Chimica Acta

Year:

2009

Language:

english

File:

PDF, 195 KB

english, 2009

50

Home treatment in paediatric patients with Hunter syndrome: the first Italian experience

Ceravolo, Ferdinando, Mascaro, Italia, Sestito, Simona, Pascale, Elisa, Lauricella, Antonino, Dizione, Elio, Concolino, Daniela

Journal:

Italian Journal of Pediatrics

Year:

2013

Language:

english

File:

PDF, 125 KB

english, 2013

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