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Results of search for 'su:"Hereditary Sensory and Motor Neuropathy"', page 15 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
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complications
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genetics
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physiology
physiopathology
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281.
Hereditary neuropathy with liability to pressure palsies and amyotrophic lateral sclerosis.
[electronic resource]
by
Bhatt, Archit
Farooq, Muhammad U
Aburashed, Rany
Kassab, Mounzer Y
Majid, Arshad
Bhatt, Shaila
Naravetla, Bharath
Dhaliwal, Gurmail
Producer:
20090914
In:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
vol. 30
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282.
Clinical Reasoning: A 15-year-old boy with bilateral wrist pain in the setting of weight loss.
[electronic resource]
by
Lau, K H Vincent
David, William S
Sadjadi, Reza
Producer:
20191119
In:
Neurology
vol. 92
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283.
Inherited motor-sensory neuropathy with upper limb predominance associated with the tropomyosin-receptor kinase fused gene.
[electronic resource]
by
Fabrizi, Gian Maria
Høyer, Helle
Taioli, Federica
Cavallaro, Tiziana
Hilmarsen, Hilde Tveitan
Squintani, Giovanna Maddalena
Zanette, Giampietro
Braathen, Geir Julius
Producer:
20210408
In:
Neuromuscular disorders : NMD
vol. 30
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284.
Hip dysplasia in hereditary motor and sensory neuropathies.
[electronic resource]
by
Pailthorpe, C A
Benson, M K
Producer:
19920813
In:
The Journal of bone and joint surgery. British volume
vol. 74
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285.
[Myotonia congenita with familial spastic paraparesis].
[electronic resource]
by
Wessel, K
Kessler, C
Rosengart, A
Kömpf, D
Producer:
19890221
In:
Der Nervenarzt
vol. 59
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286.
Hypertrophied cauda equina presenting as intradural mass: case report and review of literature.
[electronic resource]
by
Hahn, M
Hirschfeld, A
Sander, H
Producer:
19980527
In:
Surgical neurology
vol. 49
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287.
[A juvenile case of chronic inflammatory demyelinating polyradiculoneuropathy with severe onion bulb-like change mimicking hereditary neuropathy].
[electronic resource]
by
Oda, M
Udaka, F
Kubori, T
Oka, N
Kameyama, M
Producer:
20000224
In:
No to shinkei = Brain and nerve
vol. 51
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288.
Visualization of the CMT1A duplication and HNPP deletion by FISH on stretched chromosome fibers.
[electronic resource]
by
Rautenstrauss, B
Fuchs, C
Liehr, T
Grehl, H
Murakami, T
Lupski, J R
Producer:
20000926
In:
Journal of the peripheral nervous system : JPNS
vol. 2
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289.
Sensory and motor neuropathy in a Border Collie.
[electronic resource]
by
Harkin, Kenneth R
Cash, Walter C
Shelton, G Diane
Producer:
20051128
In:
Journal of the American Veterinary Medical Association
vol. 227
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290.
Hereditary neuropathy with liability to pressure palsy.
[electronic resource]
by
Paprocka, Justyna
Kajor, Maciej
Jamroz, Ewa
Jezela-Stanek, Aleksandra
Seeman, Pavel
Marszał, Elzbieta
Producer:
20070315
In:
Folia neuropathologica
vol. 44
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291.
[Distal hereditary motor neuropathy].
[electronic resource]
by
Devic, P
Petiot, P
Producer:
20120216
In:
Revue neurologique
vol. 167
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292.
A novel syndromic form of sensory-motor polyneuropathy is linked to chromosome 22q13.31-q13.33.
[electronic resource]
by
Bohlega, S
Alazami, A M
Cupler, E
Al-Hindi, H
Ibrahim, E
Alkuraya, F S
Producer:
20110308
In:
Clinical genetics
vol. 79
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293.
Mitochondrial dynamics and inherited peripheral nerve diseases.
[electronic resource]
by
Pareyson, Davide
Saveri, Paola
Sagnelli, Anna
Piscosquito, Giuseppe
Producer:
20151012
In:
Neuroscience letters
vol. 596
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294.
Diagnosis of post-operative compressive neuropathy aided by continuous adductor canal block.
[electronic resource]
by
Ardon, Alberto E
Greengrass, Roy A
Clendenen, Steven R
Producer:
20150616
In:
Pain medicine (Malden, Mass.)
vol. 15
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295.
The different ultrasound patterns in Charcot-Marie-Tooths raise the need of standardization.
[electronic resource]
by
Padua, Luca
Briani, Chiara
Producer:
20150902
In:
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
vol. 126
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296.
Clinical, electrophysiological and magnetic resonance findings in a family with hereditary neuropathy with liability to pressure palsies caused by a novel PMP22 mutation.
[electronic resource]
by
Yurrebaso, Izaskun
Casado, Oscar L
Barcena, Joseba
Perez de Nanclares, Guiomar
Aguirre, Urko
Producer:
20140910
In:
Neuromuscular disorders : NMD
vol. 24
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297.
Hand compression neuropathy: An assessment guide.
[electronic resource]
by
MacGillis, Kyle J
Mejia, Alfonso
Siemionow, Maria Z
Producer:
20170612
In:
The Journal of family practice
vol. 65
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298.
Calf enlargement in hereditary motor and sensory neuropathy.
[electronic resource]
by
De Visser, M
Hoogendijk, J E
Ongerboer, B W
Verbeeten, B J
Producer:
19900516
In:
Muscle & nerve
vol. 13
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299.
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0.
[electronic resource]
by
Simonati, Alessandro
Fabrizi, Gian Maria
Taioli, Federica
Polo, Alberto
Cerini, Roberto
Rizzuto, Nicolò
Producer:
20021227
In:
Journal of neurology
vol. 249
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300.
[Are Friedreich's disease, Charcot-Marie disease and Déjérine-Sottas disease distinct nosologic entities? Two familial cases with associated syndromes].
[electronic resource]
by
BULGARELLI, R
LEVA, R
Producer:
20030501
In:
Minerva pediatrica
vol. 6
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