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L'ottica e la Toscana : la storia dell'ottica in Toscana dal 1200 ai nostri giorni

2005

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Phase-shifting speckle interferometry: a noise reduction filter for phase unwrapping

Optical engineering, 1997-09, Vol.36 (9), p.2466

Capanni, Annalisa

1997

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High-resolution optical topography applied to ancient painting diagnostics

Optical engineering, 1995-04, Vol.34 (4), p.1219

Bertani, Duilio

1995

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INDAGINI IN TRICROMIA FALSO COLORE: UN'APPLICAZIONE AL MICROSCOPIO

OPD restauro : quaderni dell'Opificio delle pietre dure e laboratori di restauro di Firenze, 1994-01 (6), p.126-164

1994

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Moire with one grating and a photodiode array

Applied Optics, 1985-06, Vol.24 (11), p.1565

1985

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Genetic predisposition to hemophagocytic lymphohistiocytosis: Report on 500 patients from the Italian registry

Journal of allergy and clinical immunology, 2016-01, Vol.137 (1), p.188-196.e4

2016

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Molecular basis of familial hemophagocytic lymphohistiocytosis

Haematologica (Roma), 2010-04, Vol.95 (4), p.538-541

2010

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Opioid response in paediatric cancer patients and the Val158Met polymorphism of the human catechol-O-methyltransferase (COMT) gene: an Italian study on 87 cancer children and a systematic review

BMC cancer, 2019-01, Vol.19 (1), p.113-113, Article 113

2019

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Familial hemophagocytic lymphohistiocytosis may present during adulthood: clinical and genetic features of a small series

PloS one, 2012-09, Vol.7 (9), p.e44649-e44649

2012

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Familial hemophagocytic lymphohistiocytosis: when rare diseases shed light on immune system functioning

Frontiers in immunology, 2014-04, Vol.5, p.167-167

2014

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Genotype–phenotype study of familial haemophagocytic lymphohistiocytosis type 3

Journal of medical genetics, 2011-05, Vol.48 (5), p.343-352

2011

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Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 binding

Journal of allergy and clinical immunology, 2015-05, Vol.135 (5), p.1310-1318.e1

2015

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STOP Pain Project-Opioid Response in Pediatric Cancer Patients and Gene Polymorphisms of Cytokine Pathways

Pharmaceutics, 2022-03, Vol.14 (3), p.619

2022

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Familial hemophagocytic lymphohistiocytosis: a model for understanding the human machinery of cellular cytotoxicity

Cellular and molecular life sciences : CMLS, 2012-01, Vol.69 (1), p.29-40

2012

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Variations of the UNC13D gene in patients with autoimmune lymphoproliferative syndrome

PloS one, 2013-07, Vol.8 (7), p.e68045-e68045

2013

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Diagnosing XLP1 in patients with hemophagocytic lymphohistiocytosis

Journal of allergy and clinical immunology, 2014-12, Vol.134 (6), p.1381-1387.e7

2014

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STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5

Journal of medical genetics, 2010-09, Vol.47 (9), p.595-600

2010

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XLP1 inhibitory effect by 2B4 does not affect DNAM‐1 and NKG2D activating pathways in NK cells

European journal of immunology, 2014-05, Vol.44 (5), p.1526-1534

2014

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Monoallelic mutations of the perforin gene may represent a predisposing factor to childhood anaplastic large cell lymphoma

Journal of pediatric hematology/oncology, 2014-08, Vol.36 (6), p.e359-e365

2014

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Cytophagic histiocytic panniculitis, hemophagocytic lymphohistiocytosis and undetermined autoimmune disorder: reconciling the puzzle

Italian journal of pediatrics, 2014-02, Vol.40 (1), p.17-17, Article 17

2014

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A novel assay for investigation of suspected familial haemophagocytic lymphohistiocytosis

British journal of haematology, 2010-09, Vol.150 (6), p.727-730

2010

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XLP 1 inhibitory effect by 2 B 4 does not affect DNAM ‐1 and NKG 2 D activating pathways in NK cells

European journal of immunology, 2014-05, Vol.44 (5), p.1526-1534

2014

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Type A microsatellite instability in pediatric gliomas as an indicator of Turcot syndrome

European journal of human genetics : EJHG, 2009-07, Vol.17 (7), p.919-927

2009

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correspondence: A novel assay for investigation of suspected familial haemophagocytic lymphohistiocytosis

British journal of haematology, 2010-09, Vol.150 (6), p.727-730

2010

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Promoter methylation and expression analysis of MGMT in advanced pediatric brain tumors

Oncology reports, 2009-10, Vol.22 (4), p.773-779

2009

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L'ottica e la Toscana : la storia dell'ottica in Toscana dal 1200 ai nostri giorni

Phase-shifting speckle interferometry: a noise reduction filter for phase unwrapping

High-resolution optical topography applied to ancient painting diagnostics

INDAGINI IN TRICROMIA FALSO COLORE: UN'APPLICAZIONE AL MICROSCOPIO

Moire with one grating and a photodiode array

Genetic predisposition to hemophagocytic lymphohistiocytosis: Report on 500 patients from the Italian registry

Molecular basis of familial hemophagocytic lymphohistiocytosis

Opioid response in paediatric cancer patients and the Val158Met polymorphism of the human catechol-O-methyltransferase (COMT) gene: an Italian study on 87 cancer children and a systematic review

Familial hemophagocytic lymphohistiocytosis may present during adulthood: clinical and genetic features of a small series

Familial hemophagocytic lymphohistiocytosis: when rare diseases shed light on immune system functioning

Genotype–phenotype study of familial haemophagocytic lymphohistiocytosis type 3

Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 binding

STOP Pain Project-Opioid Response in Pediatric Cancer Patients and Gene Polymorphisms of Cytokine Pathways

Familial hemophagocytic lymphohistiocytosis: a model for understanding the human machinery of cellular cytotoxicity

Variations of the UNC13D gene in patients with autoimmune lymphoproliferative syndrome

Diagnosing XLP1 in patients with hemophagocytic lymphohistiocytosis

STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5

XLP1 inhibitory effect by 2B4 does not affect DNAM‐1 and NKG2D activating pathways in NK cells

Monoallelic mutations of the perforin gene may represent a predisposing factor to childhood anaplastic large cell lymphoma

Cytophagic histiocytic panniculitis, hemophagocytic lymphohistiocytosis and undetermined autoimmune disorder: reconciling the puzzle

A novel assay for investigation of suspected familial haemophagocytic lymphohistiocytosis

XLP 1 inhibitory effect by 2 B 4 does not affect DNAM ‐1 and NKG 2 D activating pathways in NK cells

Type A microsatellite instability in pediatric gliomas as an indicator of Turcot syndrome

correspondence: A novel assay for investigation of suspected familial haemophagocytic lymphohistiocytosis

Promoter methylation and expression analysis of MGMT in advanced pediatric brain tumors

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