Results 61 to 70 of about 946 (107)

A murine model of Barth syndrome recapitulates human cardiac and skeletal muscle phenotypes. [PDF]

Dis Model Mech
Yazawa E, Keating EM, Wang S, Sweat ME, Ma Q, Xu Y, Schlame M, Pu WT.   +7 more
europepmc   +1 more source

Endovascular Therapy for Post-Thrombotic Syndrome - A Randomized Trial. [PDF]

N Engl J Med
Vedantham S, Kahn SR, Marston WA, Weinberg I, Sista AK, Magnuson EA, Cohen DJ, Wasan SM, Razavi MK, Goldhaber SZ, Sanfilippo KM, Comerota AJ, Azene EM, Chaar CIO, Leung DA, Kolli KP, Kalva SP, Rostambeigi N, Desai A, Desai KR, Tafur AJ, Khalsa B, Majerus E, Wang B, Wang Y, Nieters P, Derfler MC, Oliver A, Hardy C, Bashir R, Winokur R, Weger N, Khaja MS, Sharma A, Mani N, Kavali P, Thukral S, Lake LL, Mikkelsen K, Parpia S, C-TRACT Trial Investigators.   +40 more
europepmc   +1 more source

Contemporary insights into elamipretide's mitochondrial mechanism of action and therapeutic effects. [PDF]

Biomed Pharmacother
Sabbah HN, Alder NN, Sparagna GC, Bruce JE, Stauffer BL, Chao LH, Pitceathly RDS, Maack C, Marcinek DJ.   +8 more
europepmc   +1 more source

Granulocyte Colony Stimulating Factor (G-CSF) and Olfactory Function-A Clinical Pilot Study. [PDF]

Laryngoscope Investig Otolaryngol
Hintschich CA, Resler K, Brückner C, Altundag A, Trautmann K, Hölig K, Kroschinsky F, Pieniak M, Hummel T.   +8 more
europepmc   +1 more source

Signs and symptoms of carriers of non-<i>DMD</i> X-linked neuromuscular diseases: A scoping review. [PDF]

J Neuromuscul Dis
Simons J, Dekker A, Govaarts R, Sarkozy A, Windpassinger C, Houwen S, Voermans N.   +6 more
europepmc   +1 more source

The recurrent p.Glu3Lys variant in <i>EHHADH</i> is responsible for Fanconi syndrome with early liver dysfunction and mitochondrial abnormalities. [PDF]

Mol Genet Metab Rep
Rollier P, Cospain A, Barth M, Milon V, Gueguen N, Homedan C, Desquiret V, Bris C, Colin E, Damaj L, Ryckewaert A, Reynier P, Odent S, Amati-Bonneau P, Procaccio V, Bonneau D, Ziegler A.   +16 more
europepmc   +1 more source

Clinical and genetic spectrum of pediatric mitochondrial disorders in China: insights from a 47-case genetically confirmed cohort. [PDF]

Orphanet J Rare Dis
Yang F, Yao R, Chang G, Hu J, Feng B, Wang L, Hu F, Huang Y, Wu S, Yu T, Ding Y, Wang X.   +11 more
europepmc   +1 more source

Management of patients with post Covid-19 condition in France: A qualitative study exploring nurses' contributions to care pathways. [PDF]

J Public Health Res
Kamdem OL, Guyot J, Dupre C, Gouttefarde P, Vericel MP, Fanget M, Nguefeu Nkenfou C, Hupin D, Roche F, Botelho-Nevers E, Bongue B.   +10 more
europepmc   +1 more source

Use of nailfold capillaroscopy for evaluation of disease activity in juvenile dermatomyositis: Results of a two-center retrospective study. [PDF]

World J Clin Pediatr
Podzolkova V, Avrusin IS, Nikolaeva M, Afonina E, Davtian S, Nurseitova A, Kravtsova K, Malahova A, Yakovlev AA, Avrusin SL, Kalashnikova OV, Chasnyk VG, Kostik MM.   +12 more
europepmc   +1 more source