R. Santorelli: search on Z-Library

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1

Die heilende Kraft der Achtsamkeit

Kabat-Zinn, Jon, Santorelli, Saki, Meibert, Petra, Wild-Regel, Angelika

Journal:

PiD - Psychotherapie im Dialog

Year:

2006

Language:

german

File:

PDF, 148 KB

german, 2006

2

Use of Macrolane VRF 30 in Emicircumferential Penis Enlargement

Sito, G., Marlino, S., Santorelli, A.

Journal:

Aesthetic Surgery Journal

Year:

2013

Language:

english

File:

PDF, 2.38 MB

english, 2013

3

Delivery and Effectiveness of a Dual Language (English/Spanish) Mindfulness-Based Stress Reduction (MBSR)

Kabat-Zinn, Jon, de Torrijos, Fernando, Skillings, Anne H., Blacker, Melissa, Mumford, George T., Alvares, Danielle Levi, Santorelli, Saki, Rosal, Milagros C.

Journal:

Mindfulness & Compassion

Year:

2016

Language:

english

File:

PDF, 368 KB

english, 2016

4

The Long-Term Stability of Early Maladaptive Schemas

Lawrence P. Riso, Shoshana E. Froman, Mona Raouf, Phillip Gable, Rachel E. Maddux, Noëlle Turini-Santorelli, Suzanne Penna, Jaime A. Blandino, Carli H. Jacobs, Melissa Cherry

Journal:

Cognitive Therapy and Research

Year:

2006

Language:

english

File:

PDF, 349 KB

english, 2006

5

‘Enjoy your death’: leadership lessons forged in the crucible of organizational death and rebirth infused with mindfulness and mastery

Santorelli, Saki F.

Journal:

Contemporary Buddhism

Year:

2011

Language:

english

File:

PDF, 144 KB

english, 2011

6

What defines mindfulness-based programs? The warp and the weft

Crane, R. S., Brewer, J., Feldman, C., Kabat-Zinn, J., Santorelli, S., Williams, J. M. G., Kuyken, W.

Journal:

Psychological Medicine

Year:

2017

Language:

english

File:

PDF, 197 KB

english, 2017

7

Effectivenes of a Meditation-Based Stress Reduction Program in the Treatment of Anxiety Disorders

Kabat-Zinn, Jon, Massion, Ann O., Kristeller, Jean K., Peterson, Linda Gay, Fletcher, Kenneth E., Pbert, Lori, Lenderking, William R., Santorelli, Saki F.

Journal:

American Journal of Psychiatry

Year:

1992

Language:

english

File:

PDF, 1.68 MB

english, 1992

8

Mindfulness and Medicine

Saki Santorelli

Journal:

EXPLORE: The Journal of Science and Healing

Year:

2007

Language:

english

File:

PDF, 3.44 MB

english, 2007

9

Late adult-onset adrenomyeloneuropathy evolving with atypical severe frontal lobe syndrome: Importance of neuroimaging

Dato, Clemente, Capaldo, Guglielmo, Terracciano, Chiara, Napolitano, Filomena, D'Amico, Alessandra, Pappatà, Sabina, Santorelli, Filippo Maria, Di Iorio, Giuseppe, Sampaolo, Simone, Melone, Mariarosa

Journal:

Radiology Case Reports

Year:

2019

Language:

english

File:

PDF, 1.14 MB

english, 2019

10

Flexible Sixteen Antenna Array for Microwave Breast Cancer Detection

Bahrami, Hadi, Porter, Emily, Santorelli, Adam, Gosselin, Benoit, Popovich, Milica, Rusch, Leslie

Journal:

IEEE Transactions on Biomedical Engineering

Year:

2015

Language:

english

File:

PDF, 1.97 MB

english, 2015

11

Review:Une nouvelle introduction aux évangiles synoptiques

Review by: Paola Santorelli

Journal:

Rhetorica A Journal of the History of Rhetoric

Year:

2011

File:

PDF, 129 KB

2011

12

Seven novel mutations in the ORNT1 gene (SLC25A15) in patients with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome

S. Salvi, C. Dionisi-Vici, E. Bertini, M. Verardo, F.M. Santorelli

Journal:

Year:

2001

Language:

english

File:

PDF, 122 KB

english, 2001

13

Clinical, ultrastructural, and molecular studies in a patient with Kufs disease

Moro, Francesca, Gismondi, Floriana, Pezzini, Francesco, Santorelli, Filippo M., Simonati, Alessandro

Journal:

Neurological Sciences

Year:

2014

Language:

english

File:

PDF, 264 KB

english, 2014

14

Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome in adulthood: a rare recognizable condition

Filosto, Massimiliano, Alberici, Antonella, Tessa, Alessandra, Padovani, Alessandro, Santorelli, Filippo M.

Journal:

Neurological Sciences

Year:

2013

Language:

english

File:

PDF, 278 KB

english, 2013

15

Alexithymia and Executive Function in Younger and Older Adults

Santorelli, Gennarina D., Ready, Rebecca E.

Journal:

The Clinical Neuropsychologist

Year:

2015

Language:

english

File:

PDF, 387 KB

english, 2015

16

Standardized Practice Reduces Complications in Breast Augmentation: Results with the First 290 Consecutive Cases Versus Non-standardized Comparators

Santorelli, Adriano, Rossano, Ferdinando, Cagli, Barbara, Avvedimento, Stefano, Ghanem, Ali, Marlino, Sergio

Journal:

Aesthetic Plastic Surgery

Year:

2018

Language:

english

File:

PDF, 7.26 MB

english, 2018

17

Muscle pain in mitochondrial diseases: a picture from the Italian network

Filosto, Massimiliano, Cotti Piccinelli, Stefano, Lamperti, Costanza, Mongini, Tiziana, Servidei, Serenella, Musumeci, Olimpia, Tonin, Paola, Santorelli, Filippo Maria, Simoncini, Costanza, Primiano,

Journal:

Journal of Neurology

Year:

2019

Language:

english

File:

PDF, 854 KB

english, 2019

18

Bleeding in Plastic-Aesthetic Surgery: A Prognostic Pathway with Clinical Application

Avvedimento, Stefano, Madonna, Gabriele, Santorelli, Adriano

Journal:

Aesthetic Plastic Surgery

Year:

2020

File:

PDF, 155 KB

2020

19

Genetic heterogeneity of myoclonus epilepsy with ragged-red fibers syndrome

Filippo M. Santorelli, Carlo Casali

Journal:

Year:

1998

Language:

english

File:

PDF, 88 KB

english, 1998

20

Mitochondrial myopathy mimicking fibromyalgia syndrome

Marcello Villanova, Enrico Selvi, Alessandro Malandrini, Carlo Casali, Filippo M Santorelli, Renato De Stefano, Roberto Marcolongo

Journal:

Year:

1999

Language:

english

File:

PDF, 238 KB

english, 1999

21

Progressive exercise intolerance associated with a new muscle-restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene

Claudio Bruno, Filippo M. Santorelli, Stefania Assereto, Emmanuel Tonoli, Alessandra Tessa, Monica Traverso, Sara Scapolan, Massimo Bado, Silvana Tedeschi, Carlo Minetti

Journal:

Year:

2003

Language:

english

File:

PDF, 129 KB

english, 2003

22

HHH syndrome (hyperornithinaemia, hyperammonaemia, homocitrullinuria), with fulminant hepatitis-like presentation

S. Fecarotta, G. Parenti, P. Vajro, A. Zuppaldi, R. Della Casa, M. T. Carbone, A. Correra, G. Torre, S. Riva, C. Dionisi-Vici, F. M. Santorelli, G. Andria

Journal:

Journal of Inherited Metabolic Disease

Year:

2006

Language:

english

File:

PDF, 187 KB

english, 2006

23

A mitochondrial ATPase 6 mutation is associated with Leigh syndrome in a family and affects proton flow and adenosine triphosphate output when modeled in Escherichia coli

R Carrozzo, T Rizza, S Lucioli, R Pierini, E Bertini, FM Santorelli

Journal:

Acta Paediatrica

Year:

2004

Language:

english

File:

PDF, 336 KB

english, 2004

24

Two novel mutations of the human Δ7-sterol reductase (DHCR7) gene in children with Smith–Lemli–Opitz syndrome

C. Patrono, C. Dionisi-Vici, A. Giannotti, B. Bembi, M.C. Digilio, C. Rizzo, C. Purificato, C. Martini, R. Pierini, F.M. Santorelli

Journal:

Molecular and Cellular Probes

Year:

2002

Language:

english

File:

PDF, 120 KB

english, 2002

25

Involvement of the mitochondrial compartment in human NCL fibroblasts

Francesco Pezzini, Floriana Gismondi, Alessandra Tessa, Paola Tonin, Rosalba Carrozzo, Sara E. Mole, Filippo M. Santorelli, Alessandro Simonati

Journal:

Biochemical and Biophysical Research Communications

Year:

2011

Language:

english

File:

PDF, 816 KB

english, 2011

26

A new mtDNA–tRNAGlu mutation (14728T > C) presenting a late-onset mitochondrial encephalomyopathy

Célia Nogueira, João Nunes, Teresinha Evangelista, Fabiana Fattori, Alessandra Tessa, Cristina Pereira, Filippo M. Santorelli, Laura Vilarinho

Journal:

Year:

2007

Language:

english

File:

PDF, 304 KB

english, 2007

27

Biochemical and genetic analysis of Leigh syndrome with complex I deficiency

Dina A. Mehaney⁎, Fayza A. Hassan, Laila A. Selim, Sawsn A. Hassan, Enrico Bertini, Fillipo Santorelli, Fabiana Fattori, Randa Sabry, Reham Zeyada

Journal:

Year:

2011

Language:

english

File:

PDF, 68 KB

english, 2011

28

Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I–II loop

F. Cricchi, C. Di Lorenzo, G.S. Grieco, C. Rengo, A. Cardinale, M. Racaniello, F.M. Santorelli, G. Nappi, F. Pierelli, C. Casali

Journal:

Journal of the Neurological Sciences

Year:

2007

Language:

english

File:

PDF, 195 KB

english, 2007

29

Identification of a novel TTC19 mutation in a Portuguese family with complex III deficiency

Célia Nogueira, José Barros, Maria José Sá, Luísa Azevedo, Filippo M. Santorelli, Laura Vilarinho

Journal:

Year:

2012

Language:

english

File:

PDF, 69 KB

english, 2012

30

“Double-trouble” or digenic disorder in complex I deficiency

Lígia S. Almeida, Mariana Ferreira, Célia Nogueira, Fátima Furtado, Teresinha Evangelista, Filippo M. Santorelli, Laura Vilarinho

Journal:

Year:

2012

Language:

english

File:

PDF, 54 KB

english, 2012

31

Mitochondrial DNA depletion syndromes: an update

Federica Deodato, Simona Lucioli, Cristiano Rizzo, Maria Chiara Meschini, Filippo M. Santorelli, Enrico Bertini, Carlo Dionisi-Vici, Rosalba Carrozzo

Journal:

Paediatrics and Child Health

Year:

2009

Language:

english

File:

PDF, 221 KB

english, 2009

32

Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy

Filippo Maria Santorelli, Barbara Garavaglia…

Journal:

Orphanet Journal of Rare Diseases

Year:

2013

Language:

english

File:

PDF, 259 KB

english, 2013

33

Individual Variation of Whinnies Reflects Differences in Membership Between Spider Monkey (Ateles geoffroyi) Communities

Santorelli, Claire J., Aureli, Filippo, Ramos-Fernández, Gabriel, Schaffner, Colleen M.

Journal:

International Journal of Primatology

Year:

2013

Language:

english

File:

PDF, 286 KB

english, 2013

34

The upstream Variable Number Tandem Repeat polymorphism of the monoamine oxidase type A gene influences trigeminal pain-related evoked responses

Di Lorenzo, Cherubino, Daverio, Andrea, Pasqualetti, Patrizio, Coppola, Gianluca, Giannoudas, Ioannis, Barone, Ylenia, Grieco, Gaetano S., Niolu, Cinzia, Pascale, Esterina, Santorelli, Filippo M., Nic

Journal:

European Journal of Neuroscience

Year:

2014

Language:

english

File:

PDF, 361 KB

english, 2014

35

Novel mutation in the mitochondrial transfer RNACys gene in a child with vomiting and migraine

Almeida, Lígia S., Martins, Esmeralda, Santorelli, Filippo M., Vilarinho, Laura

Journal:

Year:

2013

Language:

english

File:

PDF, 45 KB

english, 2013

36

A novel SUCLA2 mutation in a Portuguese patient

Nogueira, Célia, Garcia, Paula, Diogo, Luísa, Valongo, Carla, Santorelli, Filippo M., Vilarinho, Laura

Journal:

Year:

2013

Language:

english

File:

PDF, 81 KB

english, 2013

37

De novo mutations inSPG3A: a challenge in differential diagnosis and genetic counselling

Leonardi, Luca, Marcotulli, Christian, Santorelli, Filippo M., Tessa, Alessandra, Casali, Carlo

Journal:

Neurological Sciences

Year:

2015

Language:

english

File:

PDF, 155 KB

english, 2015

38

The relationship between early life modifiable risk factors for childhood obesity, ethnicity and body mass index at age 3 years: findings from the Born in Bradford birth cohort study

Fairley, Lesley, Santorelli, Gillian, Lawlor, Debbie A, Bryant, Maria, Bhopal, Raj, Petherick, Emily S, Sahota, Pinki, Greenwood, Darren C, Hill, Andrew J, Cameron, Noel, Ball, Helen, Barber, Sally, W

Journal:

Year:

2015

Language:

english

File:

PDF, 434 KB

english, 2015

39

Book Review: Seneca e le scienze naturali, edited by Marco Beretta, Francesco Citti and Lucia Pasetti 

Santorelli, Biagio

Journal:

Early Science and Medicine

Year:

2015

Language:

english

File:

PDF, 53 KB

english, 2015

40

Leigh-type neuropathology in Pearson syndrome associated with impaired ATP production and a novel mtDNA deletion

Santorelli, F.M., Barmada, M.A., Pons, R., Zhang, L.L., DiMauro, S.

Journal:

Year:

1996

Language:

english

File:

PDF, 554 KB

english, 1996

41

Migraine-like disorder segregating with mtDNA 14484 Leber hereditary optic neuropathy mutation

Cupini, L. M., Massa, R., Floris, R., Manenti, G., Martini, B., Tessa, A., Nappi, G., Bernardi, G., Santorelli, F. M.

Journal:

Year:

2003

Language:

english

File:

PDF, 417 KB

english, 2003

42

Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family

Casali, C., Bonifati, V., Santorelli, F.M., Casari, G., Fortini, D., Patrignani, A., Fabbrini, G., Carrozzo, R., D'Amati, G., Locuratolo, N., Vanacore, N., Damiano, M., Pierallini, A., Pierelli, F., A

Journal:

Year:

2001

Language:

english

File:

PDF, 1.20 MB

english, 2001

43

A Novel SUCLA2 Mutation in a Portuguese Child Associated With "Mild" Methylmalonic Aciduria

Nogueira, C., Meschini, M. C., Nesti, C., Garcia, P., Diogo, L., Valongo, C., Costa, R., Videira, A., Vilarinho, L., Santorelli, F. M.

Journal:

Journal of Child Neurology

Year:

2015

Language:

english

File:

PDF, 317 KB

english, 2015

44

The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndrome

Carrozzo, R., Tessa, A., Vazquez-Memije, M.E., Piemonte, F., Patrono, C., Malandrini, A., Dionisi-Vici, C., Vilarinho, L., Villanova, M., Schagger, H., Federico, A., Bertini, E., Santorelli, F.M.

Journal:

Year:

2001

Language:

english

File:

PDF, 1.24 MB

english, 2001

45

Acute optic neuropathy associated with a novelMFN2mutation

Leonardi, Luca, Marcotulli, Christian, Storti, Eugenia, Tessa, Alessandra, Serrao, Mariano, Parisi, Vincenzo, Santorelli, F. M., Pierelli, Francesco, Casali, Carlo

Journal:

Journal of Neurology

Year:

2015

Language:

english

File:

PDF, 317 KB

english, 2015

46

Spectrum of Brain Changes in Patients With Congenital Muscular Dystrophy and FKRP Gene Mutations

Mercuri, Eugenio, Topaloglu, Haluk, Brockington, Martin, Berardinelli, Angela, Pichiecchio, Anna, Santorelli, Filippo, Rutherford, Mary, Talim, Beril, Ricci, Enzo, Voit, Thomas, Muntoni, Francesco

Journal:

Archives of Neurology

Year:

2006

Language:

english

File:

PDF, 291 KB

english, 2006

47

Clinical and molecular findings in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

Salvi, S., Santorelli, F. M., Bertini, E., Boldrini, R., Meli, C., Donati, A., Burlina, A. B., Rizzo, C., Di Capua, M., Fariello, G., Dionisi-Vici, C.

Journal:

Year:

2001

Language:

english

File:

PDF, 1.67 MB

english, 2001

48

Targeted Gene Resequencing (Astrochip) to Explore the Tripartite Synapse in Autism–Epilepsy Phenotype with Macrocephaly

Marchese, Maria, Valvo, Giulia, Moro, Francesca, Sicca, Federico, Santorelli, Filippo M.

Journal:

NeuroMolecular Medicine

Year:

2016

Language:

english

File:

PDF, 735 KB

english, 2016

49

Hereditary spastic paraplegia: pathology, genetics and therapeutic prospects

Di Fabio, Roberto, Storti, Eugenia, Tessa, Alessandra, Pierelli, Francesco, Morani, Federica, Santorelli, Filippo M.

Journal:

Expert Opinion on Orphan Drugs

Year:

2016

Language:

english

File:

PDF, 885 KB

english, 2016

50

Association between hyperglycaemia and adverse perinatal outcomes in south Asian and white British women: analysis of data from the Born in Bradford cohort

Farrar, Diane, Fairley, Lesley, Santorelli, Gillian, Tuffnell, Derek, Sheldon, Trevor A, Wright, John, van Overveld, Lydia, Lawlor, Debbie A

Journal:

The Lancet Diabetes & Endocrinology

Year:

2015

Language:

english

File:

PDF, 294 KB

english, 2015

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