Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1996 1
2000 1
2005 1
2010 1
2018 1
2019 2
2023 0

Text availability

Article attribute

Article type

Publication date

Search Results

6 results

Results by year

Filters applied: . Clear all
Page 1
The teratogenic effects of thalidomide on limbs.
Vargesson N. Vargesson N. J Hand Surg Eur Vol. 2019 Jan;44(1):88-95. doi: 10.1177/1753193418805249. Epub 2018 Oct 18. J Hand Surg Eur Vol. 2019. PMID: 30335598 Review.
Indeed phocomelia, the severe reduction or loss of the proximal long bones with retention of the distal hand/foot plate remains the stereotypical image of thalidomide. This review focuses on the type and range of damage thalidomide caused to the limbs, reviews current unde …
Indeed phocomelia, the severe reduction or loss of the proximal long bones with retention of the distal hand/foot plate remains the stereoty …
Human genetic disorders of axon guidance.
Engle EC. Engle EC. Cold Spring Harb Perspect Biol. 2010 Mar;2(3):a001784. doi: 10.1101/cshperspect.a001784. Cold Spring Harb Perspect Biol. 2010. PMID: 20300212 Free PMC article. Review.
This article reviews symptoms and signs of aberrant axon connectivity in humans, and summarizes major human genetic disorders that result, or have been proposed to result, from defective axon guidance. These include corpus callosum agenesis, L1 syndrome, Joubert syndrom
This article reviews symptoms and signs of aberrant axon connectivity in humans, and summarizes major human genetic disorders that result, o …
[Advances in research of synergistic divergence].
Chen LP, Hao R, Zhang W. Chen LP, et al. Zhonghua Yan Ke Za Zhi. 2019 Jan 11;55(1):63-67. doi: 10.3760/cma.j.issn.0412-4081.2019.01.015. Zhonghua Yan Ke Za Zhi. 2019. PMID: 30641676 Review. Chinese.
This causes the affected eye to move further into abduction on gaze to the normal side and results in extreme divergence of both eyes. It is sometimes referred to as exotropic Duane syndrome with synergistic divergence (type 4 Duane syndrome) or …
This causes the affected eye to move further into abduction on gaze to the normal side and results in extreme divergence of both eyes. It is …
Duane's retraction syndrome: literature review.
Gurwood AS, Terrigno CA. Gurwood AS, et al. Optometry. 2000 Nov;71(11):722-6. Optometry. 2000. PMID: 11101130 Review.
BACKGROUND: Duane's retraction syndrome (DRS), also known as Stilling-Turk-Duane syndrome, is defined as a congenital miswiring of the lateral and medial recti muscles, resulting in an impaired ocular motility syndrome that includes palpe …
BACKGROUND: Duane's retraction syndrome (DRS), also known as Stilling-Turk-Duane syndrome, is defined as …
[Epidemiological and clinical aspects of Stilling-Turk-Duane syndrome].
Mehel E, Quére MA, Lavenant F, Pechereau A. Mehel E, et al. J Fr Ophtalmol. 1996;19(8-9):533-42. J Fr Ophtalmol. 1996. PMID: 8944136 Review. French.
BASIS: In a retrospective study on 155 patients with Stilling-Turk-Duane's syndrome, we compare our results with those described in the literature. ...The syndrome was unilateral in 121 cases (78.1%). The left eye (71.9%) was affected more frequently t …
BASIS: In a retrospective study on 155 patients with Stilling-Turk-Duane's syndrome, we compare our results with those describ …
[Congenital fibrosis of extraocular muscles (CFEOM) and other phenotypes of congenital cranial dysinnervation syndromes (CCDD)].
Hanisch F, Bau V, Zierz S. Hanisch F, et al. Nervenarzt. 2005 Apr;76(4):395-402. doi: 10.1007/s00115-004-1742-3. Nervenarzt. 2005. PMID: 15221064 Review. German.
Within the scope of an overview, the case of a 60-year-old patient with congenital fibrosis of extraocular muscles type 1 (CFEOM1) with autosomal dominant inheritance and typical phenotype, but additional progression of the ocular symptoms, is presented. ...Further …
Within the scope of an overview, the case of a 60-year-old patient with congenital fibrosis of extraocular muscles type 1 (CFE …