Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2002 | 1 |
2014 | 1 |
2015 | 1 |
2016 | 1 |
2019 | 1 |
2022 | 1 |
2024 | 0 |
Search Results
5 results
Results by year
Filters applied: . Clear all
The following term was not found in PubMed: Martinez-Chenoll
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Update on the Clinical, Radiographic, and Neurobehavioral Manifestations in FXTAS and FMR1 Premutation Carriers.
Cerebellum. 2016 Oct;15(5):578-86. doi: 10.1007/s12311-016-0799-4.
Cerebellum. 2016.
PMID: 27287737
Free PMC article.
Review.
Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome.
Baker EK, Arpone M, Vera SA, Bretherton L, Ure A, Kraan CM, Bui M, Ling L, Francis D, Hunter MF, Elliott J, Rogers C, Field MJ, Cohen J, Maria LS, Faundes V, Curotto B, Morales P, Trigo C, Salas I, Alliende AM, Amor DJ, Godler DE.
Baker EK, et al. Among authors: maria ls.
J Neurodev Disord. 2019 Dec 26;11(1):41. doi: 10.1186/s11689-019-9288-7.
J Neurodev Disord. 2019.
PMID: 31878865
Free PMC article.
Item in Clipboard
Clinical Relevance of Liver Involvement in the Clinical Course of Systemic Sclerosis.
Lorena M, Bellan M, Lepore M, Sola D, Pedrazzoli R, Rigamonti C, De Benedittis C, Manfredi GF, Acquaviva A, Tonello S, Rizzi M, Minisini R, Pirisi M, Sainaghi PP.
Lorena M, et al.
J Clin Med. 2022 Feb 12;11(4):966. doi: 10.3390/jcm11040966.
J Clin Med. 2022.
PMID: 35207242
Free PMC article.
Item in Clipboard
Molecular classes in 209 patients with Prader-Willi or Angelman syndromes: lessons for genetic counseling.
Faundes V, María LS, Aliaga S, Curotto B, Pugin A, Alliende MA.
Faundes V, et al. Among authors: maria ls.
Am J Med Genet A. 2015 Jan;167A(1):261-3. doi: 10.1002/ajmg.a.36801. Epub 2014 Oct 6.
Am J Med Genet A. 2015.
PMID: 25287901
No abstract available.
Item in Clipboard
A frameshift insertion in the cone cyclic nucleotide gated cation channel causes complete achromatopsia in a consanguineous family from a rural isolate.
Rojas CV, María LS, Santos JL, Cortés F, Alliende MA.
Rojas CV, et al. Among authors: maria ls.
Eur J Hum Genet. 2002 Oct;10(10):638-42. doi: 10.1038/sj.ejhg.5200856.
Eur J Hum Genet. 2002.
PMID: 12357335
Item in Clipboard
Cite
Cite