domingo, 6 de enero de 2019

Genetic testing AND (genetic OR genomic) AND review - PubMed - NCBI

Genetic testing AND (genetic OR genomic) AND review - PubMed - NCBI

DNA testing concept with DNA strand and magnifier.

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PubMed comprises more than 27 million citations for biomedical literature from MEDLINE, life science journals, and online books. Citations may include links to full-text content from PubMed Central and publisher web sites.


Best matches for Genetic testing AND (genetic OR genomic) AND review:

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Items: 1 to 20 of 17738

1.
Deconstructing cortical folding: genetic, cellular and mechanical determinants.
Llinares-Benadero C, Borrell V.
Nat Rev Neurosci. 2019 Jan 4. doi: 10.1038/s41583-018-0112-2. [Epub ahead of print] Review.

PMID:
 
30610227
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2.
[Clinical Hematology for Specialists of Clinical Laboratory Medicine].
Sueoka E.
Rinsho Byori. 2016 Aug;64(8):965-971. English, Japanese.

PMID:
 
30609340
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3.
[Developing Diagnostic Tests for Infectious Diseases -MALDI-TOF MS and Genetic Diagnosis -].
Yanagihara K.
Rinsho Byori. 2016 Aug;64(8):942-953. English, Japanese.

PMID:
 
30609337
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4.
[Education and Career Development of Laboratory Personnel through Qualification System of Molecular Analysis Technologist and Specialist}.
Miyachi H.
Rinsho Byori. 2016 Aug;64(8):927-931. English, Japanese.

PMID:
 
30609334
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5.
[Accreditation of Medical Laboratory under International Standards in Clinical Trial].
Miyachi H.
Rinsho Byori. 2016 Aug;64(8):905-909. English, Japanese.

PMID:
 
30609330
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6.
DYT-GNAL.
Deutschländer AB, Wszolek ZK.
In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews®[Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2019 Jan 3.

PMID:
 
30605297
 
Free Books & Documents
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7.
Tempering aversive/traumatic memories with cannabinoids: a review of evidence from animal and human studies.
Lisboa SF, Vila-Verde C, Rosa J, Uliana DL, Stern CAJ, Bertoglio LJ, Resstel LB, Guimaraes FS.
Psychopharmacology (Berl). 2019 Jan 2. doi: 10.1007/s00213-018-5127-x. [Epub ahead of print] Review.

PMID:
 
30604182
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8.
Pheochromocytoma and paraganglioma-an update on diagnosis, evaluation, and management.
Jain A, Baracco R, Kapur G.
Pediatr Nephrol. 2019 Jan 2. doi: 10.1007/s00467-018-4181-2. [Epub ahead of print] Review.

PMID:
 
30603807
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9.
Diagnosis of monogenic chronic kidney diseases.
Armstrong ME, Thomas CP.
Curr Opin Nephrol Hypertens. 2018 Dec 28. doi: 10.1097/MNH.0000000000000486. [Epub ahead of print]

PMID:
 
30601180
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10.
Challenging the Current Recommendations for Carrier Testing in Children.
VanNoy GE, Genetti CA, McGuire AL, Green RC, Beggs AH, Holm IA; BabySeq Project Group.
Pediatrics. 2019 Jan;143(Suppl 1):S27-S32. doi: 10.1542/peds.2018-1099F.

PMID:
 
30600268
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11.
Ethical and Psychosocial Issues in Whole Genome Sequencing (WGS) for Newborns.
Lantos JD.
Pediatrics. 2019 Jan;143(Suppl 1):S1-S5. doi: 10.1542/peds.2018-1099B.

PMID:
 
30600264
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12.
Maternal uniparental isodisomy for chromosome 6 discovered by paternity testing: a case report.
Kerr ER, Stuhlmiller GM, Maha GC, Ladd MA, Mikhail FM, Koester RP, Hurst ACE.
Mol Cytogenet. 2018 Dec 20;11:60. doi: 10.1186/s13039-018-0411-3. eCollection 2018.

PMID:
 
30598700
 
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13.
Update on the diagnosis, treatment and management of rare genetic lipid disorders.
Ng DM, Burnett JR, Bell DA, Hegele RA, Hooper AJ.
Pathology. 2018 Dec 28. pii: S0031-3025(18)30571-3. doi: 10.1016/j.pathol.2018.11.005. [Epub ahead of print] Review.

PMID:
 
30598327
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14.
ASCO 2018 NSCLC highlights-combination therapy is key.
Gamerith G, Kocher F, Rudzki J, Pircher A.
Memo. 2018;11(4):266-271. doi: 10.1007/s12254-018-0444-7. Epub 2018 Oct 22. Review.

PMID:
 
30595752
 
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15.
Prenatal diagnosis of sex chromosome mosaicism with two marker chromosomes in three cell lines and a review of the literature.
Zheng J, Yang X, Lu H, Guan Y, Yang F, Xu M, Li M, Ji X, Wang Y, Hu P, Zhou Y.
Mol Med Rep. 2018 Dec 24. doi: 10.3892/mmr.2018.9798. [Epub ahead of print]

PMID:
 
30592288
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16.
MicroRNAs in pancreatic cancer diagnosis and therapy.
Słotwiński R, Lech G, Słotwińska SM.
Cent Eur J Immunol. 2018;43(3):314-324. doi: 10.5114/ceji.2018.80051. Epub 2018 Oct 30. Review.

PMID:
 
30588176
 
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17.
Resistant Cytomegalovirus Infection in Solid-organ Transplantation: Single-center Experience, Literature Review of Risk Factors, and Proposed Preventive Strategies.
Majeed A, Latif A, Kapoor V, Sohail A, Florita C, Georgescu A, Zangeneh T.
Transplant Proc. 2018 Dec;50(10):3756-3762. doi: 10.1016/j.transproceed.2018.02.091. Epub 2018 Oct 26.

PMID:
 
30586840
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18.
Genetic predisposition to colorectal cancer: syndromes, genes, classification of genetic variants and implications for precision medicine.
Valle L, Vilar E, Tavtigian SV, Stoffel EM.
J Pathol. 2018 Dec 25. doi: 10.1002/path.5229. [Epub ahead of print] Review.

PMID:
 
30584801
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19.
Microarray analysis has no additive value in fetal aberrant right subclavian artery: description of 268 pregnancies and systematic literature review.
Sagi-Dain L, Singer A, Sagi J, Amir P, Lev D, Nasser Samra N, Bar-Shira A, Zeligson S, Idit M, Ben-Shachar S.
Ultrasound Obstet Gynecol. 2018 Dec 24. doi: 10.1002/uog.20208. [Epub ahead of print]

PMID:
 
30584678
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20.
Triplet CFTR modulators: future prospects for treatment of cystic fibrosis.
Chaudary N.
Ther Clin Risk Manag. 2018 Dec 6;14:2375-2383. doi: 10.2147/TCRM.S147164. eCollection 2018. Review.

PMID:
 
30584312
 
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