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Results of search for 'su:"Hereditary Sensory and Motor Neuropathy"', page 16 of 60
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Authors
Auer-Grumbach, Michaela
Bouche, P
Brice, A
Chance, P F
De Jonghe, P
De Jonghe, Peter
Gabreëls, F J
Gabreëls-Festen, A A
Harding, A E
King, R H
LeGuern, E
Lupski, J R
Martin, J J
Nelis, E
Pareyson, D
Suter, U
Thomas, P K
Timmerman, V
Timmerman, Vincent
Van Broeckhoven, C
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Adolescent
Adult
Aged
Charcot-Marie-Tooth Disease
Child
Female
Hereditary Sensory and Motor Neuropathy
Humans
Male
Middle Aged
Mutation
Myelin Proteins
Neural Conduction
Pedigree
complications
diagnosis
genetics
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physiology
physiopathology
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Results
301.
Classification of employment factors according to the International Classification of Functioning, Disability and Health in patients with neuromuscular diseases: a systematic review.
[electronic resource]
by
Minis, Marie-Antoinette
Heerkens, Yvonne
Engels, Josephine
Oostendorp, Rob
van Engelen, Baziel
Producer:
20100223
In:
Disability and rehabilitation
vol. 31
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302.
Quality of life is not impaired in patients with hereditary neuropathy with liability to pressure palsies.
[electronic resource]
by
Padua, L
Pazzaglia, C
Cavallaro, T
Commodari, I
Pareyson, D
Quattrone, A
Rizzuto, N
Vita, G
Tonali, P A
Schenone, A
Producer:
20070319
In:
European journal of neurology
vol. 14
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303.
Coexistence of transthyretin familial amyloid polyneuropathy and hereditary neuropathy with liability to pressure palsy.
[electronic resource]
by
Conceição, Isabel
Nzwalo, Hipólito
de Carvalho, Mamede
Producer:
20130531
In:
Clinical neurology and neurosurgery
vol. 114
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304.
Sural nerve pathology in TFG-associated motor neuron disease with sensory neuropathy.
[electronic resource]
by
Li, Jia
Meng, Lingchao
Wu, Rui
Xie, Zhiying
Gang, Qiang
Zhang, Wei
Wang, Zhaoxia
Yuan, Yun
Producer:
20191224
In:
Neuropathology : official journal of the Japanese Society of Neuropathology
vol. 39
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305.
Phe 84 deletion of the PMP22 gene associated with hereditary motor and sensory neuropathy HMSN III with multiple cranial neuropathy: clinical, neurophysiological and magnetic resonance imaging findings.
[electronic resource]
by
Yener, G G
Guiochon-Mantel, A
Obuz, F
Baklan, B
Oztürk, V
Kovanlikaya, I
Cakmur, R
Genç, A
Producer:
20011004
In:
Journal of neurology
vol. 248
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306.
A misdiagnosis of multifocal motor neuropathy.
[electronic resource]
by
Pandian, Jeyaraj D
Khosla, Pooja
Producer:
20030828
In:
The Lancet. Neurology
vol. 2
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307.
Familial, demyelinating sensory and motor polyneuropathy with conduction block.
[electronic resource]
by
Scelsa, Stephen N
Producer:
20100412
In:
Muscle & nerve
vol. 41
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308.
The puzzle of TRPV4 channelopathies.
[electronic resource]
by
Nilius, Bernd
Voets, Thomas
Producer:
20130722
In:
EMBO reports
vol. 14
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309.
The broad clinical spectrum of hereditary neuropathy with liability to pressure palsy (HNPP).
[electronic resource]
by
Nascimento, Osvaldo J M
Producer:
20160826
In:
Arquivos de neuro-psiquiatria
vol. 74
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310.
Novel mutations in HINT1 gene cause autosomal recessive axonal neuropathy with neuromyotonia in two cases of sensorimotor neuropathy and one case of motor neuropathy.
[electronic resource]
by
Meng, Lingchao
Fu, Jun
Lv, He
Zhang, Wei
Wang, Zhaoxia
Yuan, Yun
Producer:
20191023
In:
Neuromuscular disorders : NMD
vol. 28
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311.
A Case of Severe Early-Onset Neuropathy Caused by a Compound Heterozygous Deletion of the PMP22 Gene: Clinical and Neurographic Aspects.
[electronic resource]
by
D'Arrigo, Stefano
Tessarollo, Valeria
Taroni, Franco
Baratta, Silvia
Pantaleoni, Chiara
Schiaffi, Elena
Ciano, Claudia
Producer:
20210507
In:
Neuropediatrics
vol. 51
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312.
Familial spastic paraplegia with neuropathy and poikiloderma. A new syndrome?
[electronic resource]
by
Antiñolo, G
Nieto, M
Borrego, S
Sierra, J
Rufo, M
Siljeström, M L
Producer:
19920807
In:
Clinical genetics
vol. 41
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313.
[Visual and somatosensory evoked potentials in hereditary motor-sensory neuropathies].
[electronic resource]
by
Nevsímalová, S
Ponca, I
Fiksa, J
Producer:
19900207
In:
Ceskoslovenska neurologie a neurochirurgie
vol. 52
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314.
Juvenile-onset of Dejerine-Sottas disease in a Taiwanese woman.
[electronic resource]
by
Liao, Y S
Chen, S T
Tang, L M
Ro, L S
Producer:
19961224
In:
Journal of the Formosan Medical Association = Taiwan yi zhi
vol. 95
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315.
Familial autosomal-dominant carpal tunnel syndrome presenting in a 5-year-old case.
[electronic resource]
by
Stögbauer, F
Young, P
Funke, H
Producer:
19980410
In:
Muscle & nerve
vol. 21
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316.
[Computer-supported tissue characterization in musculoskeletal ultrasonography].
[electronic resource]
by
Pohle, R
Fischer, D
von Rohden, L
Producer:
20010308
In:
Ultraschall in der Medizin (Stuttgart, Germany : 1980)
vol. 21
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317.
Creatine monohydrate does not increase strength in patients with hereditary neuropathy.
[electronic resource]
by
Doherty, T J
Lougheed, K
Markez, J
Tarnopolsky, M A
Producer:
20020103
In:
Neurology
vol. 57
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318.
Congenital neuropathy with the absence of large myelinated fibers.
[electronic resource]
by
Fukuda, M
Morimoto, T
Suzuki, Y
Kida, K
Ohnishi, A
Producer:
20001220
In:
Pediatric neurology
vol. 23
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319.
Bell's palsy and hereditary neuropathy with liability to pressure palsy (HNPP): is there a common genetic background?
[electronic resource]
by
Karadima, Georgia
Kokotis, Panagiotis
Kalfakis, Nikolaos
Vassilopoulos, Dimitris
Panas, Marios
Producer:
20140116
In:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
vol. 20
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320.
Bilateral Vestibulopathy Aggravates Balance and Gait Disturbances in Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis: A Case Report.
[electronic resource]
by
van Leeuwen, Roeland B
Smits, Bart W
Rodenburg, Richard J
van Engelen, Baziel G
Producer:
20170313
In:
Journal of clinical neuromuscular disease
vol. 18
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