Results 101 to 110 of about 11,481 (144)

Is Impaired Sleep Quality a Triggering Factor in Melasma Patients? A Cross-Sectional Study. [PDF]

Indian J Dermatol
Avcı C, Akın G, Akarsu S, İlknur T.
europepmc   +1 more source

Eribulin-induced resolution of high-risk basal cell carcinoma: implications for microtubule-targeting agents in BCC management: a case report. [PDF]

Acta Oncol
Lapins J, Radros N, Schultz K, Vassilaki I, Linder Stragliotto C, Helgadottir H.   +5 more
europepmc   +1 more source

Loss of primary cilia in late pituitary organogenesis does not cause endocrine dysfunction. [PDF]

J Anat
Byun K, Lin Y, Li FQ, Takemaru KI, Cheung LYM.   +4 more
europepmc   +1 more source

Submaximal Eccentric Training During Immobilization Does Not Prevent Serial Sarcomere Loss or Impairments in Mechanical Function in Old or Young Rats. [PDF]

J Gerontol A Biol Sci Med Sci
Hinks A, Vlemmix E, Power GA.
europepmc   +1 more source

Prenatal Diagnosis of Joubert Syndrome 23 With Left Isomerism: A Novel Phenotype Associated With Pathogenic KIAA0586 Variant. [PDF]

Prenat Diagn
Casteleyn T, Vogt M, Weichert A, Zimmer B, Lala B, Henrich W, Königbauer JT.   +6 more
europepmc   +1 more source

Discussing Conflicting Explanatory Approaches in Flexibility Training Under Consideration of Physiology: A Narrative Review. [PDF]

Sports Med
Warneke K, Behm DG, Alizadeh S, Hillebrecht M, Konrad A, Wirth K.   +5 more
europepmc   +1 more source

Eccentric Exercise and Muscle Damage: An Introductory Guide. [PDF]

J Funct Morphol Kinesiol
Paschalis V, Margaritelis NV, Chatzinikolaou PN, Theodorou AA, Nikolaidis MG.   +4 more
europepmc   +1 more source

A deep intronic IFT172 variant causing pseudoexon inclusion identified by whole-genome sequencing in nephronophthisis. [PDF]

CEN Case Rep
Sy PM, Baba M, Fujiwara K, Yamamura N, Kawato K, Nishi E, Aoyama S, Kimura Y, Inoki Y, Nagano C, Sakakibara N, Horinouchi T, Yamamura T, Ishimori S, Morisada N, Nozu K.   +15 more
europepmc   +1 more source

The Extrachromosomal DNA Fusion Factory: Extrachromosomal Genesis of Oncogenic Fusion Transcripts. [PDF]

Research (Wash D C)
Maimaitiyiming Y, Yang C, Hua Naranmandura.   +2 more
europepmc   +1 more source

Case Report: Clinical phenotypes and recombinant human growth hormone therapeutic exploration for a patient with Takenouchi-Kosaki syndrome harboring the <i>CDC42</i> p.Arg68Gln variant. [PDF]

Front Pediatr
Lin XX, Song YY, Xue JC, Liu H.
europepmc   +1 more source