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Regenerative and Resorbable PLA/HA Hybrid Construct for Tendon/Ligament Tissue Engineering

Annals of biomedical engineering, 2020-02, Vol.48 (2), p.757-767

2020

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Consideraciones éticas en el diagnóstico presintomático de ataxias espinocerebelosas autosómico dominantes

Neurología (Barcelona, Spain), 2017-09, Vol.32 (7), p.469-475

2017

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Ethical considerations in presymptomatic diagnosis of autosomal dominant spinocerebellar ataxias

Neurologia (Barcelona, Spain), 2017-09, Vol.32 (7), p.469

2017

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Influence of the substrate's hydrophilicity on the in vitro Schwann cells viability

Journal of biomedical materials research. Part A, 2007-11, Vol.83A (2), p.463-470

2007

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A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp

British journal of dermatology (1951), 2005-12, Vol.153 (6), p.1216-1219

2005

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Differential Expression and Processing of Chromogranin A and Secretogranin II in Relation to the Secretory Status of Endocrine Cells

Endocrinology (Philadelphia), 2006-03, Vol.147 (3), p.1408-1418

2006

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Gelatin microparticles aggregates as three-dimensional scaffolding system in cartilage engineering

Journal of materials science. Materials in medicine, 2013-02, Vol.24 (2), p.503-513

2013

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Wide clinical spectrum in Zimmermann-Laband syndrome

Genetic counseling, 2011, Vol.22 (1), p.1

2011

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Ethical considerations in presymptomatic diagnosis of autosomal dominant spinocerebellar ataxias

Neurología (Barcelona, English ed. ), 2017-09, Vol.32 (7), p.469-475

2017

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Camptodactyly, joint contractures, facial, and skeletal defects: Further delineation of the Rozin camptodactyly syndrome

American journal of medical genetics. Part A, 2006-06, Vol.140A (11), p.1245-1249

2006

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Fibrin-chitosan composite substrate for in vitro culture of chondrocytes

Journal of biomedical materials research. Part A, 2013-02, Vol.101A (2), p.404-412

2013

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Zimmermann-Laband syndrome: further clinical delineation

Genetic counseling, 2005, Vol.16 (3), p.283

2005

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Familial iridogoniodysgenesis and skeletal anomalies: a probable new autosomal recessive disorder

Clinical genetics, 2004-07, Vol.66 (1), p.23-29

2004

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A variant example of familial Floating-Harbor syndrome?

Genetic counseling, 2003, Vol.14 (1), p.31

2003

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Complete achromatopsia associated with skeletal anomalies: a new autosomal recessive syndrome

Genetic counseling, 2004, Vol.15 (4), p.455

2004

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Identification of Novel Genes Involved in the Plasticity of Pituitary Melanotropes in Amphibians

Annals of the New York Academy of Sciences, 2009-04, Vol.1163 (1), p.233-240

2009

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Chitosan microparticles for “in vitro” 3D culture of human chondrocytes

RSC advances, 2013-01, Vol.3 (18), p.6362-6368

2013

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Identification and characterization of two novel (neuro)endocrine long coiled-coil proteins

FEBS letters, 2007-07, Vol.581 (17), p.3149-3156

2007

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Acondrogénesis tipo 1A1 recurrente debida a una variante alélica del gen COL10A1?

Cirugia y cirujanos, 2019-09, Vol.87 (5)

2019

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Christian's spondylo-digital syndrome: second familial case

Clinical genetics, 1995-11, Vol.48 (5), p.268-271

1995

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Spondylo-camptodactyly syndrome: a distinct autosomal dominant entity?

Clinical genetics, 1995-10, Vol.48 (4), p.173-176

1995

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Inherited hypertrichoses

Clinical genetics, 2002-05, Vol.61 (5), p.321-329

2002

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RT-PCR analysis of the expression of POMC and its processing enzyme PC1 in amphibian melanotropes

General and comparative endocrinology, 2006-06, Vol.147 (2), p.222-230

2006

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Poland-Moebius syndrome in a boy and Poland syndrome in his mother

Clinical genetics, 1991-09, Vol.40 (3), p.225-228

1991

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Myhre syndrome: first female case

Clinical dysmorphology, 2003-04, Vol.12 (2), p.119-121

2003

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Regenerative and Resorbable PLA/HA Hybrid Construct for Tendon/Ligament Tissue Engineering

Consideraciones éticas en el diagnóstico presintomático de ataxias espinocerebelosas autosómico dominantes

Ethical considerations in presymptomatic diagnosis of autosomal dominant spinocerebellar ataxias

Influence of the substrate's hydrophilicity on the in vitro Schwann cells viability

A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp

Differential Expression and Processing of Chromogranin A and Secretogranin II in Relation to the Secretory Status of Endocrine Cells

Gelatin microparticles aggregates as three-dimensional scaffolding system in cartilage engineering

Wide clinical spectrum in Zimmermann-Laband syndrome

Ethical considerations in presymptomatic diagnosis of autosomal dominant spinocerebellar ataxias

Camptodactyly, joint contractures, facial, and skeletal defects: Further delineation of the Rozin camptodactyly syndrome

Fibrin-chitosan composite substrate for in vitro culture of chondrocytes

Zimmermann-Laband syndrome: further clinical delineation

Familial iridogoniodysgenesis and skeletal anomalies: a probable new autosomal recessive disorder

A variant example of familial Floating-Harbor syndrome?

Complete achromatopsia associated with skeletal anomalies: a new autosomal recessive syndrome

Identification of Novel Genes Involved in the Plasticity of Pituitary Melanotropes in Amphibians

Chitosan microparticles for “in vitro” 3D culture of human chondrocytes

Identification and characterization of two novel (neuro)endocrine long coiled-coil proteins

Acondrogénesis tipo 1A1 recurrente debida a una variante alélica del gen COL10A1?

Christian's spondylo-digital syndrome: second familial case

Spondylo-camptodactyly syndrome: a distinct autosomal dominant entity?

Inherited hypertrichoses

RT-PCR analysis of the expression of POMC and its processing enzyme PC1 in amphibian melanotropes

Poland-Moebius syndrome in a boy and Poland syndrome in his mother

Myhre syndrome: first female case

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