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ETMR-like infantile cerebellar embryonal tumors in the extended morphologic spectrum of DICER1-related tumors

Acta neuropathologica, 2019-01, Vol.137 (1), p.175-177

2019

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New variant (Val597Ile) in transmembrane region of the TSH receptor with human chorionic gonadotropin hypersensitivity in familial gestational hyperthyroidism

Clinical endocrinology (Oxford), 2020-09, Vol.93 (3), p.339-345

2020

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Multinodular goitre is a gateway for molecular testing of DICER1 syndrome

Clinical endocrinology (Oxford), 2019-11, Vol.91 (5), p.669-675

2019

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Acquired von Willebrand's syndrome caused by primary hypothyroidism in a 5-year-old girl

Journal of Pediatric Endocrinology and Metabolism, 2019-11, Vol.32 (11), p.1295-1298

2019

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DICER1 constitutional pathogenic variant syndrome: Where are we in 2019?

Bulletin du cancer, 2019-12, Vol.106 (12), p.1177

2019

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MiRNAs in follicular thyroid tumors

La Presse médicale (1983), 2011-07, Vol.40 (7-8), p.683-689

2011

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mtDNA controls expression of the Death Associated Protein 3

Experimental cell research, 2006-04, Vol.312 (6), p.737-745

2006

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A child with resistance to thyroid hormone without thyroid hormone receptor gene mutation: a 20-year follow-up

Thyroid (New York, N.Y.), 2008-01, Vol.18 (1), p.35-44

2008

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PGC-1-related coactivator and targets are upregulated in thyroid oncocytoma

Biochemical and biophysical research communications, 2003-10, Vol.310 (3), p.779-784

2003

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Marked hyperthyroxinemia during amiodarone treatment revealing thyroid hormone resistance syndrome

Thyroid (New York, N.Y.), 2008-09, Vol.18 (9), p.1019-1020

2008

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Syndrome associé aux variants pathogènes constitutionnels de DICER1 : Où en sommes-nous en 2019 ?

Bulletin du cancer, 2019-12, Vol.106 (12), p.1177-1189

2019

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Micro-ARNs dans les tumeurs folliculaires de la thyroïde

La Presse médicale (1983), 2011-07, Vol.40 (7-8), p.683-689

2011

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Les microARNs

Revue francophone des laboratoires, 2015-06, Vol.2015 (473), p.49-54

2015

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DICER1-associated thyroid tumour families

Endocrine Abstracts, 2024-08

2024

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Familial gestational hyperthyroidism caused by Val597ile mutant of TSH receptor gene with human chorionic gonadotropin hypersensitivity

Endocrine Abstracts, 2018-05

2018

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Long PCR Analysis of Human Gamete mtDNA Suggests Defective Mitochondrial Maintenance in Spermatozoa and Supports the Bottleneck Theory for Oocytes

Biochemical and biophysical research communications, 1998-11, Vol.252 (2), p.373-377

1998

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Resistance to thyroid hormone alpha associated with early-onset severe NASH

Endocrine Abstracts, 2019-05

2019

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A Conserved N-Terminal Sequence Targets Human DAP3 to Mitochondria

Biochemical and biophysical research communications, 2001-01, Vol.280 (1), p.177-181

2001

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A Chorionic Gonadotropin-Sensitive Mutation in the Follicle-Stimulating Hormone Receptor as a Cause of Familial Gestational Spontaneous Ovarian Hyperstimulation Syndrome

Obstetrical & gynecological survey, 2004-01, Vol.59 (1), p.37-38

2004

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Analyse de l'ADN mitochondrial humain

Annales de l'Institut Pasteur. Actualités, 2001 (9-10), p.55-70

2001

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Traitements antalgiques pour le nouveau-né en maternité et en néonatalogie (réanimation et soins intensifs exclus) : propositions thérapeutiques pratiques: Prise en charge de la douleur du nouveau-né

Médecine thérapeutique pédiatrie, 2002, Vol.5 (2), p.110-113

2002

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ETMR-like infantile cerebellar embryonal tumors in the extended morphologic spectrum of DICER1-related tumors

New variant (Val597Ile) in transmembrane region of the TSH receptor with human chorionic gonadotropin hypersensitivity in familial gestational hyperthyroidism

Multinodular goitre is a gateway for molecular testing of DICER1 syndrome

Acquired von Willebrand's syndrome caused by primary hypothyroidism in a 5-year-old girl

DICER1 constitutional pathogenic variant syndrome: Where are we in 2019?

MiRNAs in follicular thyroid tumors

mtDNA controls expression of the Death Associated Protein 3

A child with resistance to thyroid hormone without thyroid hormone receptor gene mutation: a 20-year follow-up

PGC-1-related coactivator and targets are upregulated in thyroid oncocytoma

Marked hyperthyroxinemia during amiodarone treatment revealing thyroid hormone resistance syndrome

Update of the UMD-VHL database: classification of 164 challenging variants based on genotype–phenotype correlation among 605 entries: Cancer genetics

Syndrome associé aux variants pathogènes constitutionnels de DICER1 : Où en sommes-nous en 2019 ?

Micro-ARNs dans les tumeurs folliculaires de la thyroïde

Les microARNs

DICER1-associated thyroid tumour families

Familial gestational hyperthyroidism caused by Val597ile mutant of TSH receptor gene with human chorionic gonadotropin hypersensitivity

Long PCR Analysis of Human Gamete mtDNA Suggests Defective Mitochondrial Maintenance in Spermatozoa and Supports the Bottleneck Theory for Oocytes

Resistance to thyroid hormone alpha associated with early-onset severe NASH

A Conserved N-Terminal Sequence Targets Human DAP3 to Mitochondria

A Chorionic Gonadotropin-Sensitive Mutation in the Follicle-Stimulating Hormone Receptor as a Cause of Familial Gestational Spontaneous Ovarian Hyperstimulation Syndrome

Analyse de l'ADN mitochondrial humain

Traitements antalgiques pour le nouveau-né en maternité et en néonatalogie (réanimation et soins intensifs exclus) : propositions thérapeutiques pratiques: Prise en charge de la douleur du nouveau-né

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