David N Herrmann
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Explore the profile of David N Herrmann including associated specialties, affiliations and a list of published articles.
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123
Citations
1672
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Recent Articles
1.
Bertini A, Reilly M, Pisciotta C, Previtali S, Parman Y, Battaloglu E, et al.
Eur J Neurol
. 2025 Feb;
32(2):e70084.
PMID: 39943887
Background And Aims: In 2019, we conducted a cross-sectional study, collecting information on 50 patients with CMT4B, an ultrarare CMT subtype, to better define the clinical phenotype. We now aimed...
2.
Cortese A, Dohrn M, Curro R, Negri S, Lassuthova P, Pisciotta C, et al.
Brain
. 2025 Feb;
PMID: 39938083
Biallelic loss-of-function mutations in the sorbitol dehydrogenase (SORD) gene cause the most common recessive type of Charcot-Marie-Tooth disease (CMT), CMT-SORD. However, the full genotype-phenotype spectrum and progression of the disease...
3.
Reynolds E, Koenig F, Watanabe M, Kwiatek A, Elafros M, Stino A, et al.
Ann Clin Transl Neurol
. 2024 Oct;
11(12):3115-3124.
PMID: 39394845
Objective: Compare the diagnostic characteristics of intraepidermal nerve fiber density (IENFD) and confocal corneal microscopy (CCM) for distal symmetric polyneuropathy (DSP) and small fiber neuropathy (SFN). Methods: Participants with obesity...
4.
Ahden S, Zatar W, Herrmann D, Ray Dorsey E, George B
Neurol Educ
. 2024 Oct;
3(1):e200118.
PMID: 39360147
Background And Objectives: To identify trends in educational debt for US medical school graduates entering neurology and compare debt to anticipated compensation. Methods: Data of 148 accredited medical schools were...
5.
Danzi M, Powell E, Rebelo A, Dohrn M, Beijer D, Fazal S, et al.
Exp Neurol
. 2024 Oct;
382:114978.
PMID: 39357594
In the past decade, human genetics research saw an acceleration of disease gene discovery and further dissection of the genetic architectures of many disorders. Much of this progress was enabled...
6.
Sadjadi R, Picher-Martel V, Morrow J, Thedens D, DiCamillo P, McCray B, et al.
Neurology
. 2024 Aug;
103(5):e209763.
PMID: 39133880
Background And Objectives: Charcot-Marie-Tooth disease type 4J (CMT4J) is caused by autosomal recessive variants in the () gene. Recent preclinical work has demonstrated the feasibility of adeno-associated virus serotype 9-FIG4...
7.
Anderson S, Cavaletti G, Hood L, Polydefkis M, Herrmann D, Rance G, et al.
Pharmacol Res Perspect
. 2024 Jul;
12(4):e1204.
PMID: 38969959
Reversible axonal swelling and brainstem auditory evoked potential (BAEP) changes were observed in standard chronic (9-month) toxicology studies in dogs treated with ritlecitinib, an oral Janus kinase 3/tyrosine kinase expressed...
8.
Curry P, Herrmann D, Stanton M, Mongiovi P, Akmyradov C, Logigian E
Muscle Nerve
. 2024 Jul;
70(5):1082-1088.
PMID: 38958279
Introduction/aims: Not all patients with chronic inflammatory demyelinating polyneuropathy (CIDP) have evidence of demyelination on nerve conduction studies (NCS). Patients with "supportive" evidence of CIDP on cerebrospinal fluid (CSF), magnetic...
9.
Kosmanopoulos G, Donohue J, Hoke M, Thomas S, Peyton M, Vo L, et al.
Brain
. 2024 Jun;
148(1):238-251.
PMID: 38917025
Dominant missense mutations of the calcium-permeable cation channel TRPV4 cause Charcot-Marie-Tooth disease (CMT) type 2C and two forms of distal spinal muscular atrophy. These conditions are collectively referred to as...
10.
Xu I, Danzi M, Ruiz A, Raposo J, Arcia de Jesus Y, Reilly M, et al.
J Peripher Nerv Syst
. 2024 Apr;
29(2):202-212.
PMID: 38581130
Background: Caused by duplications of the gene encoding peripheral myelin protein 22 (PMP22), Charcot-Marie-Tooth disease type 1A (CMT1A) is the most common hereditary neuropathy. Despite this shared genetic origin, there...