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1964
2025

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1964 2
1965 1
1966 1
1967 2
1972 2
1973 1
1974 1
1976 1
1979 2
1980 1
1981 1
1982 2
1983 2
1985 2
1986 1
1987 1
1988 5
1989 2
1990 3
1991 5
1992 2
1993 6
1994 2
1995 4
1996 3
1997 5
1998 10
1999 1
2000 4
2001 8
2002 6
2003 2
2004 5
2005 12
2006 1
2007 5
2008 9
2009 10
2010 8
2011 10
2012 11
2013 12
2014 14
2015 10
2016 9
2017 18
2018 16
2019 28
2020 15
2021 20
2022 6
2023 20
2024 14
2025 0

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304 results

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Page 1
Arthrogryposis Multiplex Congenita.
Langston S, Chu A. Langston S, et al. Pediatr Ann. 2020 Jul 1;49(7):e299-e304. doi: 10.3928/19382359-20200624-01. Pediatr Ann. 2020. PMID: 32674167 Review.
Arthrogryposis multiplex congenita (AMC) is a complex, etiologically diverse, clinical descriptor identified in a variety of diagnoses characterized by multiple congenital joint contractures. ...Those infants with syndromic causes of arthrogryposis are
Arthrogryposis multiplex congenita (AMC) is a complex, etiologically diverse, clinical descriptor identified in a varie
Genetic Diseases of PIEZO1 and PIEZO2 Dysfunction.
Alper SL. Alper SL. Curr Top Membr. 2017;79:97-134. doi: 10.1016/bs.ctm.2017.01.001. Epub 2017 Feb 28. Curr Top Membr. 2017. PMID: 28728825 Review.
Loss-of-function mutations in the human PIEZO2 gene cause an autosomal recessive syndrome of muscular atrophy with perinatal respiratory distress, arthrogryposis, and scoliosis. Gain-of-function mutations in the human PIEZO2 gene cause three clinical types of autosomal dom …
Loss-of-function mutations in the human PIEZO2 gene cause an autosomal recessive syndrome of muscular atrophy with perinatal respiratory dis …
Hereditary neuropathy with liability to pressure palsies.
Attarian S, Fatehi F, Rajabally YA, Pareyson D. Attarian S, et al. J Neurol. 2020 Aug;267(8):2198-2206. doi: 10.1007/s00415-019-09319-8. Epub 2019 Apr 15. J Neurol. 2020. PMID: 30989370 Review.
Early onset hereditary neuronopathies: an update on non-5q motor neuron diseases.
Zambon AA, Pini V, Bosco L, Falzone YM, Munot P, Muntoni F, Previtali SC. Zambon AA, et al. Brain. 2023 Mar 1;146(3):806-822. doi: 10.1093/brain/awac452. Brain. 2023. PMID: 36445400 Free PMC article. Review.
Of note, we are increasingly aware of the broad range of phenotypes caused by pathogenic variants in the same gene and of the considerable clinical and genetic overlap between HMN and other conditions, such as Charcot-Marie-Tooth type 2 (axonal), spinal muscular atrophy with lowe …
Of note, we are increasingly aware of the broad range of phenotypes caused by pathogenic variants in the same gene and of the considerable c …
Panorama of the distal myopathies.
Savarese M, Sarparanta J, Vihola A, Jonson PH, Johari M, Rusanen S, Hackman P, Udd B. Savarese M, et al. Acta Myol. 2020 Dec 1;39(4):245-265. doi: 10.36185/2532-1900-028. eCollection 2020 Dec. Acta Myol. 2020. PMID: 33458580 Free PMC article. Review.
However, despite being characterized by a wide clinical and genetic heterogeneity, the distal myopathies are a category of muscular dystrophies: genetic diseases with progressive loss of muscle fibers. Myopathic congenital arthrogryposis is also a form of distal myopathy u …
However, despite being characterized by a wide clinical and genetic heterogeneity, the distal myopathies are a category of muscular dystroph …
Arthrogryposis multiplex congenita: dental and maxillofacial phenotype - A scoping review.
Taqi D, Nematollahi S, Lemin S, Rauch F, Hamdy R, Dahan-Oliel N. Taqi D, et al. Bone. 2024 Feb;179:116955. doi: 10.1016/j.bone.2023.116955. Epub 2023 Nov 10. Bone. 2024. PMID: 37951521 Review.
INTRODUCTION: Arthrogryposis multiplex congenita (AMC) is a heterogeneous group of disorders associated with decreased fetal movement, with a prevalence between 1/3000 and 1/5200 live births. ...
INTRODUCTION: Arthrogryposis multiplex congenita (AMC) is a heterogeneous group of disorders associated with decreased …
Arthrogryposis multiplex congenita in utero: radiologic and pathologic findings.
Skaria P, Dahl A, Ahmed A. Skaria P, et al. J Matern Fetal Neonatal Med. 2019 Feb;32(3):502-511. doi: 10.1080/14767058.2017.1381683. Epub 2017 Sep 27. J Matern Fetal Neonatal Med. 2019. PMID: 28954562 Free article. Review.
Arthrogryposis multiplex congenita (AMC) refers to the development of multiple joint contractures affecting two or more areas of the body prior to birth. It affects approximately 1 in 3000 individuals, mostly reported in individuals of Asian, African and Euro
Arthrogryposis multiplex congenita (AMC) refers to the development of multiple joint contractures affecting two or more
Arthrogryposis multiplex congenita: classification, diagnosis, perioperative care, and anesthesia.
Ma L, Yu X. Ma L, et al. Front Med. 2017 Mar;11(1):48-52. doi: 10.1007/s11684-017-0500-4. Epub 2017 Mar 2. Front Med. 2017. PMID: 28213879 Review.
Arthrogryposis multiplex congenita (AMC) is a rare disorder characterized by non-progressive, multiple contractures. ...
Arthrogryposis multiplex congenita (AMC) is a rare disorder characterized by non-progressive, multiple contractures. ..
[Arthrogryposis multiplex congenita].
Linnet KM, Balslev T, Møller-Madsen B. Linnet KM, et al. Ugeskr Laeger. 2015 Aug 10;177(33):V12140712. Ugeskr Laeger. 2015. PMID: 26320355 Free article. Review. Danish.
Arthrogryposis multiplex congenita (AMC) is a sign rather than a diagnosis. It implies contractures in multiple body areas and occurs in 1:3,000-5,000 live births. ...
Arthrogryposis multiplex congenita (AMC) is a sign rather than a diagnosis. It implies contractures in multiple body ar
The range of publications on arthrogryposis multiplex congenita from 1995 to 2022-A scoping review.
Hermansen MV, Wekre LL, Lidal IB. Hermansen MV, et al. Am J Med Genet A. 2023 Jul;191(7):1693-1703. doi: 10.1002/ajmg.a.63201. Epub 2023 Apr 3. Am J Med Genet A. 2023. PMID: 37009761 Review.
Arthrogryposis multiplex congenita (AMC) is defined as "a group of congenital conditions characterized by joint contractures in two or more body areas." ...
Arthrogryposis multiplex congenita (AMC) is defined as "a group of congenital conditions characterized by joint contrac
304 results