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High degree of consensus on diagnosis and management of rotator cuff tears: a Delphi approach

Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA, 2023-10, Vol.31 (10), p.4594-4600

2023

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Insight into the Pathology of a COL1A1 Signal Peptide Heterozygous Mutation Leading to Severe Osteogenesis Imperfecta

Calcified tissue international, 2018-03, Vol.102 (3), p.373-379

2018

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Prise en charge multidisciplinaire et évolution d’un cas de troubles autistiques dans un contexte carentiel : implication nosographique

Neuropsychiatrie de l'enfance et de l'adolescence, 2010-04, Vol.58 (3), p.152-158

2010

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Re-ruptures and early outcomes after surgical repair of acute Achilles tendon ruptures: prospective, comparative multicenter study

International orthopaedics, 2023-07, Vol.47 (7), p.1855-1861

2023

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P168 – 2679: Intrafamilial variability in Ehlers Danlos syndrome type VI

European journal of paediatric neurology, 2015-05, Vol.19, p.S141-S141

2015

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Arthroscopic Hill-Sachs Filling Technique Using an Absorbable Interference Screw

Arthroscopy techniques (Amsterdam), 2022-12, Vol.11 (12), p.e2389-e2395

2022

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Are Schatzker and AO classifications accurate enough to classify tibial plateau fractures in alpine skiers?

International orthopaedics, 2021-07, Vol.45 (7), p.1863-1869

2021

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Ethical Challenges in COVID-19 Biospecimen Research: Perspectives From Institutional Review Board Members and Bioethicists

Mayo Clinic proceedings, 2021-01, Vol.96 (1), p.165-173

2021

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Mare's colostrum globules stimulate fibroblast growth in vitro: a biochemical study

Journal of medicinal food, 2009-08, Vol.12 (4), p.836-845

2009

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COL5A1 Haploinsufficiency Is a Common Molecular Mechanism Underlying the Classical Form of EDS

American journal of human genetics, 2000-06, Vol.66 (6), p.1766-1776

2000

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Influence of ethanol, malate and arginine on histamine production of Lactobacillus hilgardii isolated from an Italian red wine

Amino acids, 2009, Vol.36 (1), p.81-89

2009

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The 2017 international classification of the Ehlers–Danlos syndromes

American journal of medical genetics. Part C, Seminars in medical genetics, 2017-03, Vol.175 (1), p.8-26

2017

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Subtalar arthrodesis using a single compression screw: a comparison of results between anterograde and retrograde screwing

European journal of orthopaedic surgery & traumatology, 2022-12, Vol.32 (8), p.1583-1589

2022

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A cluster of autosomal recessive spondylocostal dysostosis caused by three newly identified DLL3 mutations segregating in a small village

Clinical genetics, 2003-07, Vol.64 (1), p.28-35

2003

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Morphostructural investigation of the female reproductive system and molecular evidence for Wolbachia in Balclutha brevis Lindberg 1954 (Hemiptera, Cicadellidae)

Micron (Oxford, England : 1993), 2016-02, Vol.81, p.23-33

2016

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Spondylocheiro Dysplastic Form of the Ehlers-Danlos Syndrome—An Autosomal-Recessive Entity Caused by Mutations in the Zinc Transporter Gene SLC39A13

American journal of human genetics, 2008-06, Vol.82 (6), p.1290-1305

2008

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Mutations in FKBP14 Cause a Variant of Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis, Myopathy, and Hearing Loss

American journal of human genetics, 2012-02, Vol.90 (2), p.201-216

2012

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Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of Complement

American journal of human genetics, 2016-11, Vol.99 (5), p.1005-1014

2016

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ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components

Molecular genetics and metabolism, 2013-07, Vol.109 (3), p.289-295

2013

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Characterization of 11 new mutations in COL3A1 of individuals with Ehlers-Danlos syndrome type IV: Preliminary comparison of RNase cleavage, EMC and DHPLC assays

Human mutation, 2000-08, Vol.16 (2), p.176-177

2000

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Risk Factors for Emotional/Behavioral Problems in Young Adolescents: A Prospective Analysis of Adolescent and Parental Stress and Symptoms

Journal of consulting and clinical psychology, 1989-12, Vol.57 (6), p.732-740

1989

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Mutations in PRDM5 in Brittle Cornea Syndrome Identify a Pathway Regulating Extracellular Matrix Development and Maintenance

American journal of human genetics, 2011-06, Vol.88 (6), p.767-777

2011

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Manejo odontológico de pacientes pediátricos comprometidos sistemáticamente. Revisión bibliográfica

Revista de Odontopediatria Latinoamericana, 2021-02, Vol.5 (1)

2021

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Purification and catalytic properties of two catechol 1,2-dioxygenase isozymes from benzoate-grown cells of Acinetobacter radioresistens

Journal of Protein Chemistry, 2000-11, Vol.19 (8), p.709-716

2000

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A proteomic approach to studying biogenic amine producing lactic acid bacteria

Proteomics (Weinheim), 2005-02, Vol.5 (3), p.687-698

2005

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High degree of consensus on diagnosis and management of rotator cuff tears: a Delphi approach

Insight into the Pathology of a COL1A1 Signal Peptide Heterozygous Mutation Leading to Severe Osteogenesis Imperfecta

Prise en charge multidisciplinaire et évolution d’un cas de troubles autistiques dans un contexte carentiel : implication nosographique

Re-ruptures and early outcomes after surgical repair of acute Achilles tendon ruptures: prospective, comparative multicenter study

P168 – 2679: Intrafamilial variability in Ehlers Danlos syndrome type VI

Arthroscopic Hill-Sachs Filling Technique Using an Absorbable Interference Screw

Are Schatzker and AO classifications accurate enough to classify tibial plateau fractures in alpine skiers?

Ethical Challenges in COVID-19 Biospecimen Research: Perspectives From Institutional Review Board Members and Bioethicists

Mare's colostrum globules stimulate fibroblast growth in vitro: a biochemical study

COL5A1 Haploinsufficiency Is a Common Molecular Mechanism Underlying the Classical Form of EDS

Influence of ethanol, malate and arginine on histamine production of Lactobacillus hilgardii isolated from an Italian red wine

The 2017 international classification of the Ehlers–Danlos syndromes

Subtalar arthrodesis using a single compression screw: a comparison of results between anterograde and retrograde screwing

A cluster of autosomal recessive spondylocostal dysostosis caused by three newly identified DLL3 mutations segregating in a small village

Morphostructural investigation of the female reproductive system and molecular evidence for Wolbachia in Balclutha brevis Lindberg 1954 (Hemiptera, Cicadellidae)

Spondylocheiro Dysplastic Form of the Ehlers-Danlos Syndrome—An Autosomal-Recessive Entity Caused by Mutations in the Zinc Transporter Gene SLC39A13

Mutations in FKBP14 Cause a Variant of Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis, Myopathy, and Hearing Loss

Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of Complement

ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components

Characterization of 11 new mutations in COL3A1 of individuals with Ehlers-Danlos syndrome type IV: Preliminary comparison of RNase cleavage, EMC and DHPLC assays

Risk Factors for Emotional/Behavioral Problems in Young Adolescents: A Prospective Analysis of Adolescent and Parental Stress and Symptoms

Mutations in PRDM5 in Brittle Cornea Syndrome Identify a Pathway Regulating Extracellular Matrix Development and Maintenance

Manejo odontológico de pacientes pediátricos comprometidos sistemáticamente. Revisión bibliográfica

Purification and catalytic properties of two catechol 1,2-dioxygenase isozymes from benzoate-grown cells of Acinetobacter radioresistens

A proteomic approach to studying biogenic amine producing lactic acid bacteria

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