Suchergebnisse - "Ben Aim, Laurène"

PubPharm (5)

1

International initiative for a curated SDHB variant database improving the diagnosis of hereditary paraganglioma and pheochromocytoma

enthalten in: Journal of medical genetics | 2022

von Ben Aim, L. | Maher, E. | Cascon, A. | +15

2

Targeted next-generation sequencing detects rare genetic events in pheochromocytoma and paraganglioma

enthalten in: Journal of medical genetics | 2019

von Ben Aim, L. | Pigny, P. | Castro-Vega, L. | +15

3

Positive Impact of Genetic Test on the Management and Outcome of Patients With Paraganglioma and/or Pheochromocytoma

enthalten in: The Journal of clinical endocrinology and metabolism | 2019

von Buffet, A. | Ben Aim, L. | Leboulleux, S. | +31

4

A new titinopathy : Childhood-juvenile onset Emery-Dreifuss-like phenotype without cardiomyopathy

enthalten in: Neurology | 2015

von De Cid, R. | Ben Yaou, R. | Roudaut, C. | +17

5

A new titinopathy: Childhood-juvenile onset Emery-Dreifuss–like phenotype without cardiomyopathy

enthalten in: Neurology | 2015

von De Cid, R. | Ben Yaou, R. | Roudaut, C. | +17

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