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
2004 1
2014 1
2020 1
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

4 results

Results by year

Filters applied: . Clear all
Your search was processed without automatic term mapping because it retrieved zero results.
Page 1
Prolonged survival in Edwards syndrome with congenital heart disease: a case report and literature review.
López-Ríos V, Grajales-Marín E, Gómez-Zambrano V, Barrios-Arroyave FA. López-Ríos V, et al. Medwave. 2020 Sep 3;20(8):e8015. doi: 10.5867/medwave.2020.08.8015. Medwave. 2020. PMID: 32956340 Review. English, Spanish.
Edwards syndrome or trisomy 18 is a complex entity that involves the musculoskeletal, craniofacial, cardiovascular, and neurological systems. Its genetics are varied, presenting both in a complete and mosaic type. Survival rarely exceeds the first year of lif …
Edwards syndrome or trisomy 18 is a complex entity that involves the musculoskeletal, craniofacial, cardiovascular, and neurol …
Cardiac anomalies in children with congenital duodenal obstruction: a systematic review with meta-analysis.
Pijpers AGH, Eeftinck Schattenkerk LD, de Vries R, Broers CJM, Straver B, van Heurn ELW, Musters GD, Gorter RR, Derikx JPM. Pijpers AGH, et al. Pediatr Surg Int. 2023 Mar 26;39(1):160. doi: 10.1007/s00383-023-05449-3. Pediatr Surg Int. 2023. PMID: 36967411 Free PMC article. Review.
The most prevalent type of obstruction was type 3 (complete atresias), with a pooled percentage of 54% (95% CI 0.48-0.60). The pooled percentage of Trisomy 21 in patients with DO was 28% (95% CI 0.26-0.31). CONCLUSION: This review shows cardiac anomalies are found i …
The most prevalent type of obstruction was type 3 (complete atresias), with a pooled percentage of 54% (95% CI 0.48-0.60). The pooled …
[XY type gonadal dysgenesis, trisomy X and variants].
Kikuchi I, Takeuchi H, Kinoshita K. Kikuchi I, et al. Nihon Rinsho. 2004 Feb;62(2):309-12. Nihon Rinsho. 2004. PMID: 14968537 Review. Japanese.
XY gonadal dysgenesis, this is a condition that has XY chromosome but is characterized by the indifferent testis. There are complete and incomplete types. Complete type has bilateral gonads of cordee, does not show physical characteristics of Turner's syndrome
XY gonadal dysgenesis, this is a condition that has XY chromosome but is characterized by the indifferent testis. There are complete
Bone marrow transplantation for Behçet's disease: a case report and systematic review of the literature.
Soysal T, Salihoğlu A, Esatoğlu SN, Gültürk E, Eşkazan AE, Hatemi G, Hatemi I, Öngören Aydın Ş, Erzin YZ, Başlar Z, Tüzüner N, Ferhanoğlu B, Çelik AF. Soysal T, et al. Rheumatology (Oxford). 2014 Jun;53(6):1136-41. doi: 10.1093/rheumatology/ket479. Epub 2014 Feb 6. Rheumatology (Oxford). 2014. PMID: 24505123 Review.
RESULTS: A 30-year-old woman with refractory GI BD involvement with trisomy 8 MDS underwent a successful myeloablative allogeneic HSCT resulting in complete resolution of both BD and MDS. ...All of these patients achieved complete remission of GI findings aft …
RESULTS: A 30-year-old woman with refractory GI BD involvement with trisomy 8 MDS underwent a successful myeloablative allogeneic HSC …