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

Year Number of Results
1982 2
1988 1
1990 2
1991 4
1992 1
1993 1
1994 1
1995 1
1996 3
1998 1
1999 1
2000 2
2001 4
2002 7
2003 4
2004 1
2005 4
2006 2
2007 2
2008 5
2009 4
2010 5
2011 4
2012 5
2013 10
2014 9
2015 4
2016 6
2017 4
2018 3
2019 2
2020 4
2021 4
2022 7
2023 2
2024 0

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110 results

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Page 1
Idiopathic inflammatory myopathies: a review.
Ashton C, Paramalingam S, Stevenson B, Brusch A, Needham M. Ashton C, et al. Intern Med J. 2021 Jun;51(6):845-852. doi: 10.1111/imj.15358. Intern Med J. 2021. PMID: 34155760 Review.
Idiopathic inflammatory myopathy (IIM) is the umbrella term including dermatomyositis (DM), polymyositis (PM), overlap myositis (OM), sporadic inclusion body myositis (IBM) and necrotising autoimmune myopathy (NAM), also known as immune-mediated necrotising myopathy. ...DM …
Idiopathic inflammatory myopathy (IIM) is the umbrella term including dermatomyositis (DM), polymyositis (PM), overlap myositis (OM), …
The trisomy 18 syndrome.
Cereda A, Carey JC. Cereda A, et al. Orphanet J Rare Dis. 2012 Oct 23;7:81. doi: 10.1186/1750-1172-7-81. Orphanet J Rare Dis. 2012. PMID: 23088440 Free PMC article. Review.
., increased nuchal translucency thickness, growth retardation, choroid plexus cyst, overlapping of fingers, and congenital heart defects ). The recognizable syndrome pattern consists of major and minor anomalies, prenatal and postnatal growth deficiency, an increas …
., increased nuchal translucency thickness, growth retardation, choroid plexus cyst, overlapping of fingers, and congenital he …
Myotonic Dystrophies: A Genetic Overview.
Soltanzadeh P. Soltanzadeh P. Genes (Basel). 2022 Feb 17;13(2):367. doi: 10.3390/genes13020367. Genes (Basel). 2022. PMID: 35205411 Free PMC article. Review.
There are two genetically distinct types of myotonic dystrophy: myotonic dystrophy type 1 (DM1) and myotonic dystrophy type 2 (DM2), both dominantly inherited with significant overlap in clinical manifestations. DM1 results from CTG repeat expansions in the 3'-untranslated …
There are two genetically distinct types of myotonic dystrophy: myotonic dystrophy type 1 (DM1) and myotonic dystrophy type 2 (DM2), both do …
[Trisomy 18 or postnatal Edward´s syndrome: descriptive study conducted at the University Hospital Center of Casablanca and literature review].
Outtaleb FZ, Errahli R, Imelloul N, Jabrane G, Serbati N, Dehbi H. Outtaleb FZ, et al. Pan Afr Med J. 2020 Dec 3;37:309. doi: 10.11604/pamj.2020.37.309.26205. eCollection 2020. Pan Afr Med J. 2020. PMID: 33654528 Free PMC article. Review. French.
The diagnosis of trisomy 18 should be suspected at birth in newborns with typical craniofacial dysmorphism, arms lifted in supplication and permanent flexion of the fingers, the index finger overlapping the 3(rd) finger, the little finger ove
The diagnosis of trisomy 18 should be suspected at birth in newborns with typical craniofacial dysmorphism, arms lifted in supplication and …
Functional dystonia.
Schmerler DA, Espay AJ. Schmerler DA, et al. Handb Clin Neurol. 2016;139:235-245. doi: 10.1016/B978-0-12-801772-2.00020-5. Handb Clin Neurol. 2016. PMID: 27719842 Review.
Certain regional phenotypes have been recognized as distinctive, such as unilateral lip and jaw deviation, laterocollis with ipsilateral shoulder elevation and contralateral shoulder depression, fixed wrist and finger flexion with relative sparing of the thumb and index …
Certain regional phenotypes have been recognized as distinctive, such as unilateral lip and jaw deviation, laterocollis with ipsilateral sho …
GLI3-related polydactyly: a review.
Al-Qattan MM, Shamseldin HE, Salih MA, Alkuraya FS. Al-Qattan MM, et al. Clin Genet. 2017 Nov;92(5):457-466. doi: 10.1111/cge.12952. Epub 2017 Feb 22. Clin Genet. 2017. PMID: 28224613 Review.
These four entities are: the preaxial polydactyly type IV-Greig-acrocallosal spectrum, postaxial polydactyly types A/B, Pallister-Hall syndrome (PHS), and oral-facial-digital overlap syndrome. We also provide illustrative clinical examples from our practice including a fam …
These four entities are: the preaxial polydactyly type IV-Greig-acrocallosal spectrum, postaxial polydactyly types A/B, Pallister-Hall syndr …
MRI anatomy and injuries of the fingers.
Zbojniewicz AM. Zbojniewicz AM. Pediatr Radiol. 2023 Jul;53(8):1562-1575. doi: 10.1007/s00247-023-05624-7. Epub 2023 Feb 18. Pediatr Radiol. 2023. PMID: 36808525 Review.
This article will review the anatomy pertinent to injuries at the fingers, provide protocol guidance, and discuss pathology encountered at the fingers. Although much of the encountered pathology in the fingers overlaps with adults, unique pathology to …
This article will review the anatomy pertinent to injuries at the fingers, provide protocol guidance, and discuss pathology encounter …
Soft-Tissue Tumors of the Hand-Imaging Features.
Stacy GS, Bonham J, Chang A, Thomas S. Stacy GS, et al. Can Assoc Radiol J. 2020 May;71(2):161-173. doi: 10.1177/0846537119888356. Epub 2020 Jan 22. Can Assoc Radiol J. 2020. PMID: 32063006 Review.
Imaging studies of the hands and fingers are common, and radiologists are generally comfortable with traumatic and degenerative conditions which arise frequently in daily practice. However, a variety of common and uncommon soft-tissue tumors also occur in the hand, the app …
Imaging studies of the hands and fingers are common, and radiologists are generally comfortable with traumatic and degenerative condi …
Some Reactive Lesions of Bone Are Probably Neoplasms.
Memon RA, Wei S, Siegal GP. Memon RA, et al. Arch Pathol Lab Med. 2022 Jan 1;146(1):60-69. doi: 10.5858/arpa.2020-0817-RA. Arch Pathol Lab Med. 2022. PMID: 33946096 Free article. Review.
.-: Some lesions previously thought to be reactive are locally aggressive and demonstrate reproducible molecular abnormalities, and thus may be neoplasms. Although most common in the bones of the fingers and toes, these lesions also occur in long and other bones. The clini …
.-: Some lesions previously thought to be reactive are locally aggressive and demonstrate reproducible molecular abnormalities, and thus may …
Pfeiffer syndrome.
Vogels A, Fryns JP. Vogels A, et al. Orphanet J Rare Dis. 2006 Jun 1;1:19. doi: 10.1186/1750-1172-1-19. Orphanet J Rare Dis. 2006. PMID: 16740155 Free PMC article. Review.
Type 2 consists of cloverleaf skull, extreme proptosis, finger and toe abnormalities, elbow ankylosis or synostosis, developmental delay and neurological complications. Type 3 is similar to type 2 but without a cloverleaf skull. Clinical overlap between the three ty …
Type 2 consists of cloverleaf skull, extreme proptosis, finger and toe abnormalities, elbow ankylosis or synostosis, developmental de …
110 results