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Publications by B Keren

PTPN11 Mutations in Patients With LEOPARD Syndrome: A French Multicentric Experience

Journal of Medical Genetics

English

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Cancer Risk in Patients With Noonan Syndrome Carrying a PTPN11 Mutation

European Journal of Human Genetics

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PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity

American Journal of Human Genetics

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Targetable Driver Mutations in Multicentric Reticulohistiocytosis

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Novel GRN Mutations in Patients With Corticobasal Syndrome

Scientific Reports

Multidisciplinary

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Experience in Managing Patients With Churg-Strauss Syndrome.

Medicni perspektivi (Medical perspectives)

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CYP1B1 Mutations in French Patients With Early-Onset Primary Open-Angle Glaucoma

Journal of Medical Genetics

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A Retrospective Study of 34ï¿½patients With Unicentric and Multicentric Castleman's Disease: Experience From a Single Institution

Oncology Letters

Cancer Research

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PTPN11 Mutations in Childhood Acute Lymphoblastic Leukemia Occur as a Secondary Event Associated With High Hyperdiploidy

Cancer Research

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Mutations of the ANG Gene in French Patients With Sporadic Amyotrophic Lateral Sclerosis

Archives of Neurology

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