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Pediatric reference Raman data for material characteristics of iliac trabecular bone

Bone (New York, N.Y.), 2014-12, Vol.69, p.89-97

2014

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Normative data on mineralization density distribution in iliac bone biopsies of children, adolescents and young adults

Bone (New York, N.Y.), 2009-06, Vol.44 (6), p.1043-1048

2009

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CRTAP deficiency leads to abnormally high bone matrix mineralization in a murine model and in children with osteogenesis imperfecta type VII

Bone (New York, N.Y.), 2010-03, Vol.46 (3), p.820-826

2010

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A cross-sectional multicenter study of osteogenesis imperfecta in North America - results from the linked clinical research centers

Clinical genetics, 2015-02, Vol.87 (2), p.133-140

2015

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Structural and cellular changes during bone growth in healthy children

Bone (New York, N.Y.), 2000-10, Vol.27 (4), p.487-494

2000

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Normative data for iliac bone histomorphometry in growing children

Bone (New York, N.Y.), 2000-02, Vol.26 (2), p.103-109

2000

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MEPE, the Gene Encoding a Tumor-Secreted Protein in Oncogenic Hypophosphatemic Osteomalacia, Is Expressed in Bone

Genomics (San Diego, Calif.), 2001-06, Vol.74 (3), p.342-351

2001

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Mineral particle size in children with dominant osteogenesis imperfecta is not associated with specific collagen mutation: A synchrotron X-ray scattering study

Bone (New York, N.Y.), 2012-05, Vol.50, p.S129-S129

2012

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Cortical bone material / compositional properties in growing children and young adults aged 1.5–23 years, as a function of gender, age, metabolic activity, and growth spurt

Bone (New York, N.Y.), 2022-12, Vol.165, p.116548-116548, Article 116548

2022

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The bone formation defect in idiopathic juvenile osteoporosis is surface-specific

Bone (New York, N.Y.), 2002-07, Vol.31 (1), p.85-89

2002

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Abnormally high bone mineralization in children with osteogenesis imperfecta is neither associated with specific collagen mutations nor with clinical severity of the disease

Bone (New York, N.Y.), 2009-07, Vol.45, p.S105-S105

2009

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CRTAP deficiency leads to high bone matrix mineralization in children (Osteogenesis imperfecta type VII) and mice

Bone (New York, N.Y.), 2009-06, Vol.44, p.S232-S233

2009

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Severe non-lethal recessive type viii oi: clinical, histological and radiographic features

Bone (New York, N.Y.), 2009-06, Vol.44, p.S283-S284

2009

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Incident vertebral compression 1 year following glucocorticoid initiation among children with rheumatic conditions: Results of a National Chronic Illness Osteoporosis Surveillance Program

Bone (New York, N.Y.), 2009-07, Vol.45, p.S55-S55

2009

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Short-term skeletal changes in children with newly diagnosed glucocorticoid-treated nephrotic syndrome

Bone (New York, N.Y.), 2009-07, Vol.45, p.S73-S73

2009

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Prevalent vertebral compression in children with newly diagnosed rheumatic conditions: Results of a national chronic illness osteoporosis surveillance program

Bone (New York, N.Y.), 2009-07, Vol.45, p.S73-S73

2009

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Quantitative Immunogold Labeling of Bone Sialoprotein and Osteopontin in Methylmethacrylate-embedded Rat Bone

The journal of histochemistry and cytochemistry, 2003-01, Vol.51 (1), p.61-67

2003

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Effect of gene dose and parental origin on bone histomorphometry in X-linked Hyp mice

Bone (New York, N.Y.), 2004, Vol.34 (1), p.134-139

2004

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Perspectives on the evolution of genetic counselling: Experience over three decades in a family with recurrent lethal osteogenesis imperfecta

Molecular genetics and metabolism, 2020-09, Vol.131 (1-2), p.114-115

2020

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Cesarean delivery is not associated with decreased at-birth fracture rates in osteogenesis imperfecta

Genetics in medicine, 2016-06, Vol.18 (6), p.570-576

2016

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Static and dynamic bone histomorphometry in children with osteogenesis imperfecta

Bone (New York, N.Y.), 2000-06, Vol.26 (6), p.581-589

2000

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Osteogenesis imperfecta type VII: an autosomal recessive form of brittle bone disease

Bone (New York, N.Y.), 2002-07, Vol.31 (1), p.12-18

2002

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Correction of the abnormal mineral ion homeostasis with a high-calcium, high-phosphorus, high-lactose diet rescues the PDDR phenotype of mice deficient for the 25-hydroxyvitamin D-1α-hydroxylase (CYP27B1)

Bone (New York, N.Y.), 2003-04, Vol.32 (4), p.332-340

2003

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Bone mineralization and growth are enhanced in preterm infants fed an isocaloric, nutrient-enriched preterm formula through term

The American journal of clinical nutrition, 2004-12, Vol.80 (6), p.1595-1603

2004

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Severe osteogenesis imperfecta caused by a small in‐frame deletion in CRTAP

American journal of medical genetics. Part A, 2011-11, Vol.155 (11), p.2865-2870

2011

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Pediatric reference Raman data for material characteristics of iliac trabecular bone

Normative data on mineralization density distribution in iliac bone biopsies of children, adolescents and young adults

CRTAP deficiency leads to abnormally high bone matrix mineralization in a murine model and in children with osteogenesis imperfecta type VII

A cross-sectional multicenter study of osteogenesis imperfecta in North America - results from the linked clinical research centers

Structural and cellular changes during bone growth in healthy children

Normative data for iliac bone histomorphometry in growing children

MEPE, the Gene Encoding a Tumor-Secreted Protein in Oncogenic Hypophosphatemic Osteomalacia, Is Expressed in Bone

Mineral particle size in children with dominant osteogenesis imperfecta is not associated with specific collagen mutation: A synchrotron X-ray scattering study

Cortical bone material / compositional properties in growing children and young adults aged 1.5–23 years, as a function of gender, age, metabolic activity, and growth spurt

The bone formation defect in idiopathic juvenile osteoporosis is surface-specific

Abnormally high bone mineralization in children with osteogenesis imperfecta is neither associated with specific collagen mutations nor with clinical severity of the disease

CRTAP deficiency leads to high bone matrix mineralization in children (Osteogenesis imperfecta type VII) and mice

Severe non-lethal recessive type viii oi: clinical, histological and radiographic features

Incident vertebral compression 1 year following glucocorticoid initiation among children with rheumatic conditions: Results of a National Chronic Illness Osteoporosis Surveillance Program

Short-term skeletal changes in children with newly diagnosed glucocorticoid-treated nephrotic syndrome

Prevalent vertebral compression in children with newly diagnosed rheumatic conditions: Results of a national chronic illness osteoporosis surveillance program

Quantitative Immunogold Labeling of Bone Sialoprotein and Osteopontin in Methylmethacrylate-embedded Rat Bone

Effect of gene dose and parental origin on bone histomorphometry in X-linked Hyp mice

Perspectives on the evolution of genetic counselling: Experience over three decades in a family with recurrent lethal osteogenesis imperfecta

Cesarean delivery is not associated with decreased at-birth fracture rates in osteogenesis imperfecta

Static and dynamic bone histomorphometry in children with osteogenesis imperfecta

Osteogenesis imperfecta type VII: an autosomal recessive form of brittle bone disease

Correction of the abnormal mineral ion homeostasis with a high-calcium, high-phosphorus, high-lactose diet rescues the PDDR phenotype of mice deficient for the 25-hydroxyvitamin D-1α-hydroxylase (CYP27B1)

Bone mineralization and growth are enhanced in preterm infants fed an isocaloric, nutrient-enriched preterm formula through term

Severe osteogenesis imperfecta caused by a small in‐frame deletion in CRTAP

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