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	461.	SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy. [electronic resource] by Vill, Katharina Müller-Felber, Wolfgang Gläser, Dieter Kuhn, Marius Teusch, Veronika Schreiber, Herbert Weis, Joachim Klepper, Jörg Schirmacher, Anja Blaschek, Astrid Wiessner, Manuela Strom, Tim M Dräger, Bianca Hofmeister-Kiltz, Kristina Tacke, Moritz Gerstl, Lucia Young, Peter Horvath, Rita Senderek, Jan Producer: 20181211 In: Human genetics vol. 137 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	462.	HINT1 gene pathogenic variants: the most common cause of recessive hereditary motor and sensory neuropathies in Russian patients. [electronic resource] by Shchagina, O A Milovidova, T B Murtazina, A F Rudenskaya, G E Nikitin, S S Dadali, E L Polyakov, A V Producer: 20201007 In: Molecular biology reports vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	463.	Giant axonal neuropathy in 2 siblings: a generalized disorder of intermediate filaments. [electronic resource] by Guazzi, G C Malandrini, A Gerli, R Federico, A Producer: 19910517 In: European neurology vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	464.	[Amaurosis congenita (Leber) with severe genital developmental delay]. [electronic resource] by Fehlow, P Producer: 19891122 In: Padiatrie und Grenzgebiete vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	465.	Absence of linkage of hereditary motor and sensory neuropathy type I to chromosome 1 markers. [electronic resource] by Middleton-Price, H R Harding, A E Berciano, J Pastor, J M Huson, S M Malcolm, S Producer: 19890809 In: Genomics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	466.	A novel homozygous mutation of the myelin Po gene producing Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III). [electronic resource] by Ikegami, T Nicholson, G Ikeda, H Ishida, A Johnston, H Wise, G Ouvrier, R Hayasaka, K Producer: 19960624 In: Biochemical and biophysical research communications vol. 222 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	467.	[A case of Dejerine-Sottas disease with central nervous system involvement]. [electronic resource] by Katsuragi, T Hasegawa, O Takahashi, T Kubota, H Kawauchi, Y Producer: 19930924 In: Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine vol. 82 Availability: No items available. Save to lists Add to cart (remove)
	468.	Compound heterozygous deletions of PMP22 causing severe Charcot-Marie-Tooth disease of the Dejerine-Sottas disease phenotype. [electronic resource] by Al-Thihli, Khalid Rudkin, Teresa Carson, Nancy Poulin, Chantal Melançon, Serge Der Kaloustian, Vazken M Producer: 20080911 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	469.	Recurrent takotsubo cardiomyopathy within a short span of time in a patient with hereditary motor and sensory neuropathy. [electronic resource] by Uechi, Yoichi Higa, Koichi Producer: 20090107 In: Internal medicine (Tokyo, Japan) vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	470.	Neck paraganglioma: head rotation maneuver on transcranial Doppler ultrasonography. [electronic resource] by Paschoal, Fernando Mendes Albuquerque Paschoal, Eric Homero Rogério, Ricardo Mendes Teixeira, Manoel Jacobsen Bor-Seng-Shu, Edson Producer: 20160830 In: Clinical neurology and neurosurgery vol. 137 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	471.	Wrist drop in an arcade dancing game: Unusual sudden bilateral radial palsy. [electronic resource] by Cea, Gabriel Contreras, Juan Pablo Aguilar, Shirley Vera, Julia Producer: 20200512 In: Neuromuscular disorders : NMD vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	472.	[DNA diagnosis of mitochondrial diseases is now possible]. [electronic resource] by Larsson, N G Holme, E Tulinius, M H Producer: 19900117 In: Lakartidningen vol. 86 Availability: No items available. Save to lists Add to cart (remove)
	473.	The electrophysiologic profile of Dejerine-Sottas disease (HMSN III). [electronic resource] by Benstead, T J Kuntz, N L Miller, R G Daube, J R Producer: 19900926 In: Muscle & nerve vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	474.	Simulated work performance tasks in persons with neuropathic and myopathic weakness. [electronic resource] by Kilmer, D D Aitkens, S G Wright, N C McCrory, M A Producer: 20000802 In: Archives of physical medicine and rehabilitation vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	475.	A rapid and definitive test for Charcot-Marie-Tooth 1A and hereditary neuropathy with liability to pressure palsies using multiplexed real-time PCR. [electronic resource] by Lorentzos, P Kaiser, T Kennerson, M L Nicholson, G A Producer: 20040415 In: Genetic testing vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	476.	PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies. [electronic resource] by van Paassen, Barbara W van der Kooi, Anneke J van Spaendonck-Zwarts, Karin Y Verhamme, Camiel Baas, Frank de Visser, Marianne Producer: 20141112 In: Orphanet journal of rare diseases vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	477.	Hereditary and inflammatory neuropathies: a review of reported associations, mimics and misdiagnoses. [electronic resource] by Rajabally, Yusuf A Adams, David Latour, Philippe Attarian, Shahram Producer: 20170606 In: Journal of neurology, neurosurgery, and psychiatry vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	478.	[Problems of the diagnosis and treatment of compression neuropathy of the median nerve: an analysis of typical medical practice]. [electronic resource] by Gilveg, A S Parfenov, V A Evzikov, G Yu Producer: 20190605 In: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	479.	[Giant axonal neuropathy. Presentation of 2 familial cases]. [electronic resource] by Maraví Petri, E García-Bragado, F Martín Ruiz, E Guarch, R Ruiz de Azúa, Y Yoldi, M E Producer: 19900521 In: Neurologia (Barcelona, Spain) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	480.	Nerve root and sciatic trunk enlargement in Déjérine-Sottas disease: MRI appearances. [electronic resource] by Masuda, N Hayashi, H Tanabe, H Producer: 19930319 In: Neuroradiology vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1188 results.