Context: The identification of mutations in genes encoding peptides of succinate dehydrogenase
(SDH) in pheochromocytoma/paraganglioma syndromes has necessitated clear …

1 Guan W, Ni Z, Hu Y, et al. Clinical characteristics of coronavirus disease 2019 in China. N
Engl J Med 2020; published online Feb 28. DOI: 10.1056/NEJMoa2002032. 2 Hopkins C, …

Context: Germline mutations in SDHx genes cause hereditary paraganglioma. Objective: The
aim of the study was to assess the indications for succinate dehydrogenase (SDH) genetic …

Discussion Upper respiratory tract infection is one of the most commonly identified causes
of olfactory loss, accounting for 22% to 36% of cases. 2 Herein, we describe a patient with …

The advent of endoscopic sinus surgery led to a resurgence of interest in the detailed
anatomy of the internal nose and paranasal sinuses. However, the official Terminologica …

… ; Philippe Herman, contributions to acquisition of data, accountable for all aspects of the
work in ensuring that questions related to the accuracy or integrity of any part of the work are …

Approximately 20% of patients diagnosed with a phaeochromocytoma or paraganglioma carry
a germline mutation in one of the succinate dehydrogenase (SDHx) genes (SDHA, SDHB…

Objectives: Juvenile nasopharyngeal angiofibroma often recurs if the tumor is large. This
report is a long‐term follow‐up of these cases. It establishes the prognostic values of tumor …

During the past decades, several methods (eg, electron microscopy, flow chamber experiments,
surface chemical analysis, surface charge and surface hydrophobicity measurements) …

Object The object of this study was to evaluate the natural history, pattern, and occurrence
of tumor growth and its consequences for treatment of small-sized vestibular schwannomas (…