Similar articles for PMID: 4056805

Year	Number of Results
1963	1
1968	2
1970	1
1972	3
1973	6
1974	3
1976	3
1977	1
1978	1
1979	1
1980	2
1981	2
1982	9
1983	5
1984	2
1985	4
1986	1
1987	4
1988	6
1989	2
1990	4
1991	1
1992	2
1993	3
1994	1
1995	1
1996	1
1997	1
2005	1
2006	1
2007	1
2010	2
2011	1
2014	1
2016	3
2017	1
2018	2
2019	1
2022	1
2024	0

1

A dominantly inherited lower motor neuron disorder presenting at birth with associated arthrogryposis.

Fleury P, Hageman G. Fleury P, et al. J Neurol Neurosurg Psychiatry. 1985 Oct;48(10):1037-48. doi: 10.1136/jnnp.48.10.1037. J Neurol Neurosurg Psychiatry. 1985. PMID: 4056805 Free PMC article.

2

Congenital non-progressive peripheral neuropathy with arthrogryposis multiplex.

Yuill GM, Lynch PG. Yuill GM, et al. J Neurol Neurosurg Psychiatry. 1974 Mar;37(3):316-23. doi: 10.1136/jnnp.37.3.316. J Neurol Neurosurg Psychiatry. 1974. PMID: 4364274 Free PMC article.

3

New hereditary malformation syndrome of unusual facial appearance, skeletal deformities, and musculoskeletal and sensory defects.

Middleton LT, Anastasiades V, Panayidou K, Georghiou D, Kalli E, Gabriel G, Myrianthopoulos NC. Middleton LT, et al. Am J Med Genet. 1992 Dec 1;44(6):757-61. doi: 10.1002/ajmg.1320440609. Am J Med Genet. 1992. PMID: 1481843

4

[Slowly progressive motor neuron disease associated with paralysis of the abductor muscles of the vocal cords].

Raverdy P, Richer-Bigo A. Raverdy P, et al. Rev Neurol (Paris). 1990;146(6-7):445-7. Rev Neurol (Paris). 1990. PMID: 2204989 Review. French.

5

[The arthrogrypotic syndrome].

Radu H, Stenzel K, Bene M, Török Z, Migea S, Bordeianu L, Osvath A. Radu H, et al. Dtsch Z Nervenheilkd. 1968;193(2):118-40. Dtsch Z Nervenheilkd. 1968. PMID: 4231706 German. No abstract available.

6

Arthrogryposis multiplex congenita: twenty-three cases in an Arab kindred.

Lebenthal E, Shochet SB, Adam A, Seelenfreund M, Fried A, Najenson T, Sandbank U, Matoth Y. Lebenthal E, et al. Pediatrics. 1970 Dec;46(6):891-9. Pediatrics. 1970. PMID: 5491443 No abstract available.

7

An unusual familial muscle disorder.

Cumming WJ, Kristmundsdottir F, Mahon M. Cumming WJ, et al. J Neurol Neurosurg Psychiatry. 1989 Feb;52(2):266-9. doi: 10.1136/jnnp.52.2.266. J Neurol Neurosurg Psychiatry. 1989. PMID: 2703844 Free PMC article.

8

Spinal muscular atrophy with autosomal dominant inheritance. Report of a new kindred.

Zellweger H, Simpson J, McCormick WF, Ionasescu V. Zellweger H, et al. Neurology. 1972 Sep;22(9):957-63. doi: 10.1212/wnl.22.9.957. Neurology. 1972. PMID: 4673381 No abstract available.

9

The heterogeneity of distal arthrogryposis.

Hageman G, Jennekens FG, Vette JK, Willemse J. Hageman G, et al. Brain Dev. 1984;6(3):273-83. doi: 10.1016/s0387-7604(84)80040-6. Brain Dev. 1984. PMID: 6091488

10

A dominantly inherited syndrome with continuous motor neuron discharges.

Ashizawa T, Butler IJ, Harati Y, Roongta SM. Ashizawa T, et al. Ann Neurol. 1983 Mar;13(3):285-90. doi: 10.1002/ana.410130310. Ann Neurol. 1983. PMID: 6847141

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