Results 201 to 210 of about 220,984 (248)

Clinical Heterogeneity and Candidate Biomarkers in <i>POLG</i>-Related Mitochondrial Disease. [PDF]

Neurol Genet
Bermejo-Guerrero L, Restrepo-Vera JL, Martin-Jimenez P, Navarro-Riquelme M, Garrido-Moraga R, Ochoa LE, González-Quintana A, Hernandez-Lain A, Castillo-Villalba J, Morís G, Muelas N, García-Arumí E, González V, Martínez-Sáez E, Vesperinas A, Llansó L, Juntas-Morales R, Paradas C, Kapetanovic S, Blázquez A, Martí R, Arenas J, Martín MA, Domínguez-González C.   +23 more
europepmc   +1 more source

Independent validation of transgenerational inheritance of learned pathogen avoidance in <i>Caenorhabditis elegans</i>. [PDF]

Elife
Akinosho A, Alexander J, Floyd K, Vidal-Gadea AG.   +3 more
europepmc   +1 more source

Multifactorial Predictors of Renal Outcomes in Alport Syndrome: Integrating Genetic, Clinical, and Cystic Phenotypes. [PDF]

Kidney Med
Song ZR, Li Y, Liu ZY, Li MS, Chen YQ, Lv JC, Zhou XJ, Zhang H.   +7 more
europepmc   +1 more source

Deciphering Spastic Ataxia: Clinical and Genetic Profiles. [PDF]

Neurol Genet
Damásio J, Santos M, Costa S, Moura J, Sardoeira A, Lemos C, Oliveira J, Barros J, Sequeiros J.   +8 more
europepmc   +1 more source

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Inherited Thrombophilias

Obstetrics and Gynecology Clinics of North America, 2006
Many inherited thrombophilias have been detected and the pathophysiologic insight has increased tremendously during the last decades. Despite, however, the overwhelming observational evidence on the association between inherited thrombophilia and several women's health issues, including VTE, thus far the implications for clinical practice are uncertain.
Coppens, Michiel, Kaandorp, Stef P., Middeldorp, Saskia   +2 more
openaire   +3 more sources