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Bone histomorphometry in acromegaly patients with fragility vertebral fractures

Pituitary, 2018-02, Vol.21 (1), p.56-64

2018

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Increased Gene Expression of RUNX2 and SOX9 in Mesenchymal Circulating Progenitors Is Associated with Autophagy during Physical Activity

Oxidative medicine and cellular longevity, 2019, Vol.2019, p.8426259-14

2019

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Diffuse pancreatic serous cystic neoplasm: A rare cause of pancreatic insufficiency

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2021-07, Vol.21, p.S50-S50

2021

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The clinical impact of autoimmune pancreatitis and ulcerative colitis association: A third-level, single-center italian experience

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2021-07, Vol.21, p.S38-S39

2021

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Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix

Clinical genetics, 2012-11, Vol.82 (5), p.453-459

2012

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Osteogenesis imperfecta: clinical, biochemical and molecular findings

Clinical genetics, 2006-08, Vol.70 (2), p.131-139

2006

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Osteoporosis in β-Thalassemia: Clinical and Genetic Aspects

Annals of the New York Academy of Sciences, 2005-11, Vol.1054 (1), p.451-456

2005

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Null CRTAP mutation associated with non-lethal OI and minimal collagen deposition in culture

Bone (New York, N.Y.), 2011-05, Vol.48, p.S84-S84

2011

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BOC.01.11: IMMUNOLOGICAL EFFECTS OF EXTRACELLULAR VESICLES FROM BONE MARROW-DERIVED MESENCHYMAL STEM CELLS ON A CELIAC DISEASE'S EXPERIMENTAL MODEL

Digestive and liver disease, 2024-04, Vol.56, p.S107-S107

2024

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T01.01.1 ROLE OF MIRNAS IN GASTRIC ATROPHY, AUTOIMMUNITY AND DISEASE PROGRESSION

Digestive and liver disease, 2020-10, Vol.52, p.S52

2020

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Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor, causes progressively deforming osteogenesis imperfecta with normal type I collagen

Journal of bone and mineral research, 2012-03, Vol.27 (3), p.723-728

2012

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Osteogenesis imperfecta: practical treatment guidelines

Paediatric drugs, 2000-11, Vol.2 (6), p.465-488

2000

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Relationship among VDR (BsmI and FokI), COLIA1, and CTR polymorphisms with bone mass, bone turnover markers, and sex hormones in men

Calcified tissue international, 2002-06, Vol.70 (6), p.457-462

2002

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Growth hormone treatment in osteogenesis imperfecta with quantitative defect of type I collagen synthesis

The Journal of pediatrics, 1996-09, Vol.129 (3), p.432-439

1996

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Association of CTR and COLIA1 alleles with BMD values in peri- and postmenopausal women

Calcified tissue international, 2000-11, Vol.67 (5), p.361-366

2000

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Osteogenesis imperfecta at the beginning of bone and joint decade

Croatian medical journal, 2001-08, Vol.42 (4), p.393-415

2001

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Characterization and functional analysis of cis-acting elements of the human farnesyl diphosphate synthetase (FDPS) gene 5′ flanking region

Genomics (San Diego, Calif.), 2009-03, Vol.93 (3), p.227-234

2009

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Rapid and efficient genotype analysis of the COL1A1 Sp1 binding site dimorphism, a genetic marker for bone mineral density

Molecular and cellular probes, 2002-02, Vol.16 (1), p.73-75

2002

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Detection of mutations in the ALD gene (ABCD1) in seven Italian families: Description of four novel mutations

Human mutation, 2000-09, Vol.16 (3), p.271-271

2000

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Substitution of an aspartic acid for glycine 700 in the alpha 2(I) chain of type I collagen in a recurrent lethal type II osteogenesis imperfecta dramatically affects the mineralization of bone

The Journal of biological chemistry, 1994-05, Vol.269 (20), p.14751-14758

1994

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Three novel polymorphic sequence variants in the type I collagen gene COL1A1, the main disease locus for Osteogenesis Imperfecta

Molecular and cellular probes, 2000-12, Vol.14 (6), p.329-332

2000

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Four new cases of lethal osteogenesis imperfecta due to glycine substitutions in COL1A1 and genes. Mutations in brief no. 152. Online

Human mutation, 1998, Vol.12 (1), p.71-72

1998

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A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease

Molecular and cellular probes, 2001-04, Vol.15 (2), p.75-79

2001

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Linkage analysis for prenatal diagnosis in a familial case of Stickler syndrome

Genetic counseling, 2002, Vol.13 (2), p.163

2002

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Association of BK virus with human brain tumors and tumors of pancreatic islets

International journal of cancer, 1987-01, Vol.39 (1), p.60-67

1987

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Bone histomorphometry in acromegaly patients with fragility vertebral fractures

Increased Gene Expression of RUNX2 and SOX9 in Mesenchymal Circulating Progenitors Is Associated with Autophagy during Physical Activity

Diffuse pancreatic serous cystic neoplasm: A rare cause of pancreatic insufficiency

The clinical impact of autoimmune pancreatitis and ulcerative colitis association: A third-level, single-center italian experience

Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix

Osteogenesis imperfecta: clinical, biochemical and molecular findings

Osteoporosis in β-Thalassemia: Clinical and Genetic Aspects

Null CRTAP mutation associated with non-lethal OI and minimal collagen deposition in culture

BOC.01.11: IMMUNOLOGICAL EFFECTS OF EXTRACELLULAR VESICLES FROM BONE MARROW-DERIVED MESENCHYMAL STEM CELLS ON A CELIAC DISEASE'S EXPERIMENTAL MODEL

T01.01.1 ROLE OF MIRNAS IN GASTRIC ATROPHY, AUTOIMMUNITY AND DISEASE PROGRESSION

Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor, causes progressively deforming osteogenesis imperfecta with normal type I collagen

Osteogenesis imperfecta: practical treatment guidelines

Relationship among VDR (BsmI and FokI), COLIA1, and CTR polymorphisms with bone mass, bone turnover markers, and sex hormones in men

Growth hormone treatment in osteogenesis imperfecta with quantitative defect of type I collagen synthesis

Association of CTR and COLIA1 alleles with BMD values in peri- and postmenopausal women

Osteogenesis imperfecta at the beginning of bone and joint decade

Characterization and functional analysis of cis-acting elements of the human farnesyl diphosphate synthetase (FDPS) gene 5′ flanking region

Rapid and efficient genotype analysis of the COL1A1 Sp1 binding site dimorphism, a genetic marker for bone mineral density

Detection of mutations in the ALD gene (ABCD1) in seven Italian families: Description of four novel mutations

Substitution of an aspartic acid for glycine 700 in the alpha 2(I) chain of type I collagen in a recurrent lethal type II osteogenesis imperfecta dramatically affects the mineralization of bone

Three novel polymorphic sequence variants in the type I collagen gene COL1A1, the main disease locus for Osteogenesis Imperfecta

Four new cases of lethal osteogenesis imperfecta due to glycine substitutions in COL1A1 and genes. Mutations in brief no. 152. Online

A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease

Linkage analysis for prenatal diagnosis in a familial case of Stickler syndrome

Association of BK virus with human brain tumors and tumors of pancreatic islets

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