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/vufind/Search/Results?lookfor=%22PMP22%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
/vufind/Search/Results?lookfor=%22PMP22%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
Search /vufind/Search2/Results?lookfor=%22PMP22%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
PubPharm (1.019)
1
Testing SIPA1L2 as a modifier of CMT1A using mouse models
enthalten in:
Journal of neuropathology and experimental neurology
| 2024
von
Murray, G.
|
Hines, T.
|
Tadenev, A.
| +3
UpdateOf: bioRxiv. 2023 Dec 01;:. - PMID 38076977
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2
Anesthetic Considerations for Patients with Hereditary Neuropathy with Liability to Pressure Palsies : A Narrative Review
enthalten in:
Healthcare (Basel, Switzerland)
| 2024
von
Laudanski, K.
|
Elmadhoun, O.
|
Mathew, A.
| +5
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3
Intermediate conduction velocity in two cases of Charcot-Marie-Tooth disease type 1A
enthalten in:
European journal of neurology
| 2024
von
Tomaselli, P.
|
Blake, J.
|
Polke, J.
| +4
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4
Genetic analysis of a Chinese pedigree affected with atypical Charcot-Marie-Tooth disease type 1A due to duplication of PMP22 gene
enthalten in:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
| 2024
von
Yao, L.
|
Li, M.
|
Liu, L.
| +4
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5
A study concept of expeditious clinical enrollment for genetic modifier studies in Charcot-Marie-Tooth neuropathy 1A
enthalten in:
Journal of the peripheral nervous system : JPNS
| 2024
von
Xu, I.
|
Danzi, M.
|
Ruiz, A.
| +19
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6
Enhancing the Reliability of PMP22 Copy Number Variation Detection with an Inherited Peripheral Neuropathy Panel
enthalten in:
The Journal of molecular diagnostics : JMD
| 2024
von
Lee, J.
|
Kwon, H.
|
Park, J.
| +5
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7
Recurrent Ipsilateral C5 Nerve Palsy Associated With Hereditary Neuropathy With Liability to Pressure Palsy
enthalten in:
Cureus
| 2024
von
Nozue, K.
|
Sugeno, N.
|
Ishiyama, S.
| +2
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8
Demyelination and Na+ Channel Redistribution Underlie Auditory and Vestibular Dysfunction in PMP22-Null Mice
enthalten in:
eNeuro
| 2024
von
Lee, J.
|
Park, S.
|
Perez-Flores, M.
| +8
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9
Hereditary neuropathy associated with liability to pressure palsies : a 24-year experience with carpal and cubital tunnel surgery
enthalten in:
The Journal of hand surgery, European volume
| 2024
von
François, T.
|
Davion, J.
|
Deken-Delannoy, V.
| +2
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10
An Elderly Woman with Complaints of Pain and Hearing Loss, Diagnosed with CMT1A with PMP22 Duplication
enthalten in:
Internal medicine (Tokyo, Japan)
| 2024
von
Takegami, N.
|
Hamada, M.
|
Yamaguchi-Takegami, N.
| +2
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Medienart
1.019
Aufsätze
519
E-Artikel
519
E-Ressourcen
500
Gedruckte Aufsätze
Zeitschriftentitel
41
Muscle & nerve
30
Journal of neuroscience research
28
Journal of neurology
28
Neurology
26
Journal of the peripheral nervous system : JPNS
23
Annals of the New York Academy of Sciences
23
Neuromuscular disorders : NMD
21
Brain : a journal of neurology
20
Annals of neurology
20
Human mutation
20
Neurogenetics
19
The Journal of neuroscience : the official jour...
17
Human genetics
17
Journal of neurology, neurosurgery, and psychiatry
16
Neurobiology of disease
14
Nature genetics
14
The Journal of biological chemistry
13
Human molecular genetics
12
Rinsho shinkeigaku = Clinical neurology
11
Clinical genetics
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Thema
843
Journal Article
837
Myelin Proteins
664
PMP22 protein, human
515
Research Support, Non-U.S. Gov't
198
Pmp22 protein, mouse
180
Case Reports
135
PMP22
134
Myelin P0 Protein
120
Review
103
Pmp22 protein, rat
88
Research Support, N.I.H., Extramural
82
Connexins
71
Research Support, U.S. Gov't, P.H.S.
63
RNA, Messenger
60
Comparative Study
43
DNA
42
9007-49-2
37
CMT1A
35
Charcot-Marie-Tooth disease
35
Membrane Proteins
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Erscheinungszeitraum
555
2000-
185
1900-1999
Erscheinungsjahr(e)
Von:
Bis:
Sprache
968
Englisch
22
Japanisch
15
Chinesisch
7
Französisch
3
Russisch
3
Spanisch
1
Deutsch
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