Similar articles for PMID: 15122445

Year	Number of Results
1968	1
1975	1
1988	3
1989	3
1992	2
1993	2
1994	1
1997	1
1998	1
1999	4
2000	4
2002	1
2003	1
2004	3
2005	4
2006	1
2007	4
2008	4
2009	2
2010	1
2011	4
2012	1
2013	5
2014	4
2015	11
2016	3
2017	4
2018	4
2019	1
2023	1
2024	0

1

[Progressive muscular atrophy: clinical and laboratory study in eleven patients].

Ferraz ME, Zanoteli E, Oliveira AS, Gabbai AA. Ferraz ME, et al. Arq Neuropsiquiatr. 2004 Mar;62(1):119-26. doi: 10.1590/s0004-282x2004000100021. Epub 2004 Apr 28. Arq Neuropsiquiatr. 2004. PMID: 15122445 Free article. Portuguese.

2

Unilateral progressive muscular atrophy with fast symptoms progression.

Bogucki A, Pigońska J, Szadkowska I, Gajos A. Bogucki A, et al. Neurol Neurochir Pol. 2016;50(1):52-4. doi: 10.1016/j.pjnns.2015.10.009. Epub 2015 Nov 5. Neurol Neurochir Pol. 2016. PMID: 26851691

3

A long-term prospective study of the natural course of sporadic adult-onset lower motor neuron syndromes.

Van den Berg-Vos RM, Visser J, Kalmijn S, Fischer K, de Visser M, de Jong V, de Haan RJ, Franssen H, Wokke JH, Van den Berg LH. Van den Berg-Vos RM, et al. Arch Neurol. 2009 Jun;66(6):751-7. doi: 10.1001/archneurol.2009.91. Arch Neurol. 2009. PMID: 19506135

4

[An autopsy case with lower motor neuron disease showing a transient-appearance of anti-GM1 antibody and an improvement of conduction block after gamma-globulin administration].

Kikuchi H, Kawano Y, Dohura K, Kawamura T, Taniwaki T, Yamada T, Kato M, Iwaki T, Kira J. Kikuchi H, et al. No To Shinkei. 1999 May;51(5):455-64. No To Shinkei. 1999. PMID: 10396755 Japanese.

5

Progressive Muscular Atrophy.

Liewluck T, Saperstein DS. Liewluck T, et al. Neurol Clin. 2015 Nov;33(4):761-73. doi: 10.1016/j.ncl.2015.07.005. Neurol Clin. 2015. PMID: 26515620 Review.

6

Progressive muscular atrophy variant of familial amyotrophic lateral sclerosis (PMA/ALS).

Cervenakova L, Protas II, Hirano A, Votiakov VI, Nedzved MK, Kolomiets ND, Taller I, Park KY, Sambuughin N, Gajdusek DC, Brown P, Goldfarb LG. Cervenakova L, et al. J Neurol Sci. 2000 Aug 15;177(2):124-30. doi: 10.1016/s0022-510x(00)00350-6. J Neurol Sci. 2000. PMID: 10980308 Clinical Trial.

7

Myotonia-like symptoms in a patient with spinal and bulbar muscular atrophy.

Araki K, Nakanishi H, Nakamura T, Atsuta N, Yamada S, Hijikata Y, Hashizume A, Suzuki K, Katsuno M, Sobue G. Araki K, et al. Neuromuscul Disord. 2015 Nov;25(11):913-5. doi: 10.1016/j.nmd.2015.08.006. Epub 2015 Aug 20. Neuromuscul Disord. 2015. PMID: 26363965

8

X-linked spinal and bulbar muscular atrophy (Kennedy's disease) with long-term electrophysiological evaluation: case report.

Kouyoumdjian JA, Morita Mda P, Araújo RG. Kouyoumdjian JA, et al. Arq Neuropsiquiatr. 2005 Mar;63(1):154-9. doi: 10.1590/s0004-282x2005000100028. Epub 2005 Apr 13. Arq Neuropsiquiatr. 2005. PMID: 15830083 Free article.

9

[Diagnostic difficulties in spinal muscular atrophy].

Araújo AP, Ramos VG, Cabello PH. Araújo AP, et al. Arq Neuropsiquiatr. 2005 Mar;63(1):145-9. doi: 10.1590/s0004-282x2005000100026. Epub 2005 Apr 13. Arq Neuropsiquiatr. 2005. PMID: 15830081 Free article. Portuguese.

10

Clinical profile of motor neuron disease patients with lower urinary tract symptoms and neurogenic bladder.

Vázquez-Costa JF, Arlandis S, Hervas D, Martínez-Cuenca E, Cardona F, Pérez-Tur J, Broseta E, Sevilla T. Vázquez-Costa JF, et al. J Neurol Sci. 2017 Jul 15;378:130-136. doi: 10.1016/j.jns.2017.04.053. Epub 2017 May 2. J Neurol Sci. 2017. PMID: 28566149

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