Experience in the clinical and genetic diagnosis of a series of Algerian patients with hereditary spastic paraplegias.

IF 1.6 4区医学 Q3 CLINICAL NEUROLOGY

Neurogenetics Pub Date : 2025-06-25 DOI:10.1007/s10048-025-00833-8

Mouna Messaoud-Khelifi, Razika Boulariah-Hadjou, Mohamed Islam Kediha, Lena Guillot-Noel, Marine Guillaud-Bataille, Christelle Marie Durand, Lamia Ali-Pacha, Wahiba Amer El Khedoud, Fanny Mochel, Jean-Madeleine de Sainte-Agathe, Giovanni Stevanin

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阿尔及利亚一系列遗传性痉挛性截瘫患者的临床和遗传学诊断经验。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Neurogenetics 医学-临床神经学

CiteScore

3.90

自引率

0.00%

发文量

审稿时长

6 months

期刊介绍： Neurogenetics publishes findings that contribute to a better understanding of the genetic basis of normal and abnormal function of the nervous system. Neurogenetic disorders are the main focus of the journal. Neurogenetics therefore includes findings in humans and other organisms that help understand neurological disease mechanisms and publishes papers from many different fields such as biophysics, cell biology, human genetics, neuroanatomy, neurochemistry, neurology, neuropathology, neurosurgery and psychiatry. All papers submitted to Neurogenetics should be of sufficient immediate importance to justify urgent publication. They should present new scientific results. Data merely confirming previously published findings are not acceptable.