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Hepatitis E Virus‐Induced Neurological Symptoms in a Kidney‐Transplant Patient with Chronic Hepatitis

American journal of transplantation, 2010-05, Vol.10 (5), p.1321-1324

2010

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Vocal-fold leukoplakia and dysplasia. Mini-review by the French Society of Phoniatrics and Laryngology (SFPL)

European annals of otorhinolaryngology, head and neck diseases, 2020-11, Vol.137 (5), p.399-404

2020

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Use of fluorescent in‐situ hybridisation in salivary gland cytology: A powerful diagnostic tool

Cytopathology (Oxford), 2017-08, Vol.28 (4), p.312-320

2017

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A French retrospective study on clinical outcome in 102 choroid plexus tumors in children

Journal of neuro-oncology, 2017-10, Vol.135 (1), p.151-160

2017

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Guidelines of the French Society of Otorhinolaryngology–Head and Neck Surgery (SFORL), part I: Primary treatment of pleomorphic adenoma

European annals of otorhinolaryngology, head and neck diseases, 2021-09, Vol.138 (4), p.269-274

2021

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Subventricular zones: new key targets for glioblastoma treatment

Radiation oncology (London, England), 2017-04, Vol.12 (1), p.67-67, Article 67

2017

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Molecular and clinical diversity in primary central nervous system lymphoma

Annals of oncology, 2023-02, Vol.34 (2), p.186-199

2023

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Cytopathological analysis of salivary gland cancer: REFCOR recommendations by the formal consensus method

European annals of otorhinolaryngology, head and neck diseases, 2024-03, Vol.141 (2), p.87-91

2024

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Characteristics of IDH-mutant gliomas with non-canonical IDH mutation

Journal of neuro-oncology, 2021, Vol.151 (2), p.279-286

2021

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Germline mutation p.N363K in POLE is associated with an increased risk of colorectal cancer and giant cell glioblastoma

Familial cancer, 2019-04, Vol.18 (2), p.173-178

2019

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Evidence for BRAF V600E and H3F3A K27M double mutations in paediatric glial and glioneuronal tumours

Neuropathology and applied neurobiology, 2015-04, Vol.41 (3), p.403-408

2015

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Highly Concordant Results Between Immunohistochemistry and Molecular Testing of Mutated V600E BRAF in Primary and Metastatic Melanoma

Acta dermato-venereologica, 2016, Vol.96 (5), p.630-634

2016

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Wernicke encephalopathy and Creutzfeldt-Jakob disease

Journal of neurology, 2009-06, Vol.256 (6), p.904-909

2009

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PL1.1 CDKN2A homozygous deletion is a strong adverse prognosis factor in diffuse malignant IDHmutant gliomas

Neuro-oncology (Charlottesville, Va.), 2019-09, Vol.21 (Supplement_3), p.iii1-iii1

2019

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Guidelines of the French Society of Otorhinolaryngology–Head and Neck Surgery (SFORL), part II: Management of recurrent pleomorphic adenoma of the parotid gland

European annals of otorhinolaryngology, head and neck diseases, 2021-01, Vol.138 (1), p.45-49

2021

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Carbimazole-induced juvenile dermatomyositis

British journal of dermatology (1951), 2008-01, Vol.158 (1), p.196-197

2008

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PO-0647: Subventricular zones: new key targets for glioblastoma treatment

Radiotherapy and oncology, 2016-04, Vol.119, p.S302-S303

2016

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Intracellular Ferritin Accumulation in Neural and Extraneural Tissue Characterizes a Neurodegenerative Disease Associated with a Mutation in the Ferritin Light Polypeptide Gene

Journal of neuropathology and experimental neurology, 2004-04, Vol.63 (4), p.363-380

2004

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Efficiency of targeted NGS on myopathies and muscular dystrophy genes: Importance of an optimized strategy of capture, sequencing, bioinformatic analyses and multidisciplinary approach for variants detection and interpretation

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S161-S162

2016

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Congenital neuromuscular diseases with neonatal respiratory failure excluding myotonic dystrophy type 1 and infantile spinal muscular atrophy. Diagnosis strategy according to a 19-child series

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2016-09, Vol.23 (9), p.878-886

2016

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CDKN2A homozygous deletion is a strong adverse prognosis factor in diffuse malignant IDH-mutant gliomas

Neuro-oncology (Charlottesville, Va.), 2019-07, Vol.21 (12), p.1519-1528

2019

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Detection of human cytomegalovirus genome and gene products in central nervous system tumours

British journal of cancer, 2005-02, Vol.92 (4), p.747-750

2005

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O10.02 MITOTIC INDEX, MICROVASCULAR PROLIFERATION AND NECROSIS DEFINE THREE GROUPS OF 1P/19Q CO-DELETED ANAPLASTIC OLIGODENDROGLIOMAS ASSOCIATED WITH DIFFERENT GENOMIC ALTERATIONS

Neuro-oncology (Charlottesville, Va.), 2014-09, Vol.16 (suppl 2), p.ii23-ii23

2014

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Increased exposure to statins in patients developing chronic muscle diseases: a 2-year retrospective study

Annals of the rheumatic diseases, 2008-05, Vol.67 (5), p.614-619

2008

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Desmoplastic infantile astrocytoma with benign histological phenotype and multiple intracranial localizations at presentation

Journal of neuro-oncology, 2010-05, Vol.98 (1), p.143-149

2010

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Hepatitis E Virus‐Induced Neurological Symptoms in a Kidney‐Transplant Patient with Chronic Hepatitis

Vocal-fold leukoplakia and dysplasia. Mini-review by the French Society of Phoniatrics and Laryngology (SFPL)

Use of fluorescent in‐situ hybridisation in salivary gland cytology: A powerful diagnostic tool

A French retrospective study on clinical outcome in 102 choroid plexus tumors in children

Guidelines of the French Society of Otorhinolaryngology–Head and Neck Surgery (SFORL), part I: Primary treatment of pleomorphic adenoma

Subventricular zones: new key targets for glioblastoma treatment

Molecular and clinical diversity in primary central nervous system lymphoma

Cytopathological analysis of salivary gland cancer: REFCOR recommendations by the formal consensus method

Characteristics of IDH-mutant gliomas with non-canonical IDH mutation

Germline mutation p.N363K in POLE is associated with an increased risk of colorectal cancer and giant cell glioblastoma

Evidence for BRAF V600E and H3F3A K27M double mutations in paediatric glial and glioneuronal tumours

Highly Concordant Results Between Immunohistochemistry and Molecular Testing of Mutated V600E BRAF in Primary and Metastatic Melanoma

Wernicke encephalopathy and Creutzfeldt-Jakob disease

PL1.1 CDKN2A homozygous deletion is a strong adverse prognosis factor in diffuse malignant IDHmutant gliomas

Guidelines of the French Society of Otorhinolaryngology–Head and Neck Surgery (SFORL), part II: Management of recurrent pleomorphic adenoma of the parotid gland

Carbimazole-induced juvenile dermatomyositis

PO-0647: Subventricular zones: new key targets for glioblastoma treatment

Intracellular Ferritin Accumulation in Neural and Extraneural Tissue Characterizes a Neurodegenerative Disease Associated with a Mutation in the Ferritin Light Polypeptide Gene

Efficiency of targeted NGS on myopathies and muscular dystrophy genes: Importance of an optimized strategy of capture, sequencing, bioinformatic analyses and multidisciplinary approach for variants detection and interpretation

Congenital neuromuscular diseases with neonatal respiratory failure excluding myotonic dystrophy type 1 and infantile spinal muscular atrophy. Diagnosis strategy according to a 19-child series

CDKN2A homozygous deletion is a strong adverse prognosis factor in diffuse malignant IDH-mutant gliomas

Detection of human cytomegalovirus genome and gene products in central nervous system tumours

O10.02 MITOTIC INDEX, MICROVASCULAR PROLIFERATION AND NECROSIS DEFINE THREE GROUPS OF 1P/19Q CO-DELETED ANAPLASTIC OLIGODENDROGLIOMAS ASSOCIATED WITH DIFFERENT GENOMIC ALTERATIONS

Increased exposure to statins in patients developing chronic muscle diseases: a 2-year retrospective study

Desmoplastic infantile astrocytoma with benign histological phenotype and multiple intracranial localizations at presentation

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