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Afferent Visual Pathway Affection in Patients with PMP22 Deletion-Related Hereditary Neuropathy with Liability to Pressure Palsies.

机译：pmp22缺失相关遗传性神经病患者对压力性麻痹负责的传入视觉通路影响。

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Alexander U Brandt; Elena Meinert-Bohn; Jan Leo Rinnenthal; Hanna Zimmermann; Janine Mikolajczak; Timm Oberwahrenbrock; Sebastian Papazoglou; Caspar F Pfüller; Johann Schinzel; Björn Tackenberg; Friedemann Paul; Katrin Hahn; Judith Bellmann-Strobl;
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1. Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation. [J] . Lenssen PP, Gabreels-Festen AA, Valentijn LJ, Brain: A journal of neurology . 1998,第Pta8期

机译：遗传性神经病伴有压力性麻痹。具有常见缺失和PMP22移码突变的患者之间的表型差异。
2. A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies. [J] . Muglia M, Patitucci A, Rizzi R, Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology . 2007,第1a2期

机译：意大利家庭遗传性神经病的PMP22基因的新型点突变，对压力性麻痹负责。
3. A family with a novel frameshift mutation in the PMP22 gene (c.433_434insC) causing a phenotype of hereditary neuropathy with liability to pressure palsies. [J] . Zephir H, Stojkovic T, Latour P, Neuromuscular disorders: NMD . 2005,第7期

机译：一个在PMP22基因（c.433_434insC）中具有新的移码突变的家庭，导致遗传性神经病的表型与压力性麻痹有关。
4. Dose-Optimization of Respiratory-Gated Auricular Vagal Afferent Nerve Stimulation (RAVANS) for Blood Pressure Modulation in Hypertensive Patients [C] . Jessica Stowell, Ronald G Garcia, Rachel Staley, Computing in Cardiology Conference . 2019

机译：呼吸门控耳廓迷走神经刺激（RAVANS）的剂量优化高血压患者的血压。
5. A Review of Leber Hereditary Optic Neuropathy and Stargardt's Disease: Comfort Level of Genetic Counselors in Dealing with Patients with these two Disorders [D] . Pani, Blerta 2011

机译：Leber遗传性视神经病变和Stargardt病的综述：遗传咨询员在应对这两种疾病时的舒适度
6. Afferent Visual Pathway Affection in Patients with PMP22 Deletion-Related Hereditary Neuropathy with Liability to Pressure Palsies [O] . Alexander U. Brandt, Elena Meinert-Bohn, Jan Leo Rinnenthal, -1

机译：PMP22缺失相关遗传性神经病患者对压力性瘫痪的传入视觉通路影响
7. A newly identified Thr99fsX110 mutation in the PMP22 gene associated with an atypical phenotype of the hereditary neuropathy with liability to pressure palsies. [O] . Izabela Moszyńska, Dagmara Kabzińska, Elena Sinkiewicz-Darol, 2009

机译：对PMP22基因的新鉴定的THR99FSX110突变与遗传性神经病变的非典型表型，对压力麻痹的责任。

Afferent Visual Pathway Affection in Patients with PMP22 Deletion-Related Hereditary Neuropathy with Liability to Pressure Palsies.

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