Results 51 to 60 of about 48,388 (151)
Mucocele is an uncommon pathology of the vermiform appendix estimated to be seen in 0.2-0.3%. The term mucocele means dilation of the appendix due to mucus, caused either by a benign or a malignant process. Herein, we report the case of a 77-year-old man
Hanen Loukil +3 more
doaj +1 more source
Taxane-induced morphea in a patient with CREST syndrome
The taxanes, docetaxel and paclitaxel, are microtubule stabilizing chemotherapeutic agents that have demonstrated antineoplastic effects in a variety of solid tumors.
Susan Michele Bouchard +2 more
doaj +1 more source
Induction of Neural Crest Stem Cells From Bardet–Biedl Syndrome Patient Derived hiPSCs
Neural crest cells arise in the embryo from the neural plate border and migrate throughout the body, giving rise to many different tissue types such as bones and cartilage of the face, smooth muscles, neurons, and melanocytes.
William B. Barrell +42 more
doaj +1 more source
CREST Syndrome with Pulmonary Arterial Hypertension
A 79-year-old woman was admitted to our hospital with effort dyspnea. Plain radiographs of the chest showed an enlargement of the heart and pleural fluid (Picture 1). Echocardiography showed remarkable right heart loading (Picture 2). Pulmonary arterial hypertension (PAH) and right heart failure manifesting hepatomegaly, ascites, jugular venous ...
Fukuda, Yusuke +2 more
openaire +3 more sources
Recurrent uveitis in a patient with CREST syndrome: a case report. [PDF]
Khalayli N +4 more
europepmc +1 more source
Dis3l2 is essential for neural crest survival by modulating Akt signaling
DIS3-like 3’-5’ exoribonuclease 2 (DIS3L2), an exoribonuclease, is known to preferentially degrade uridylated RNA substrates, miRNAs, and ncRNAs. Recent reports show that DIS3L2 also plays a key role in cell proliferation and tumor growth.
Sian D’Silva +2 more
doaj +1 more source
CREST Syndrome in Systemic Sclerosis Patients - Is Dystrophic Calcinosis a Key Element to a Positive Diagnosis? [PDF]
Bobeica C +16 more
europepmc +1 more source
Síndrome de CREST. Presentación de un caso CREST syndrome. Presentation of a case
Como esclerodermia, se designa un grupo de enfermedades y síndromes que tienen como característica común la induración y el engrosamiento cutáneos.
Yanet Acosta Piedra +4 more
doaj
Placode and neural crest origins of congenital deafness in mouse models of Waardenburg-Shah syndrome
Summary: Mutations in the human genes encoding the endothelin ligand-receptor pair EDN3 and EDNRB cause Waardenburg-Shah syndrome (WS4), which includes congenital hearing impairment. The current explanation for auditory dysfunction is defective migration
Jaime Tan +3 more
doaj +1 more source
Biventricular affection in CREST syndrome
Marcus, Brugger +4 more
openaire +2 more sources

