Results 51 to 60 of about 46,735 (152)
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 Associated with Pulmonary Hypertension.
52歳の女性。初診の10年前に,顔面,頚部,四肢の色素沈着,5,6年前に,手指の腫脹,硬化,屈曲困難,1年前に,Raynaud症状が出現。8年前より胸部X線にて心拡大を指摘。6ヵ月前に,労作時息切れ,心胸郭比63.2%,肝腫大等の心不全症状が出現。10日前より起座呼吸となり,2001年1月15日,当院内科入院。心エコーで肺動脈収縮期圧81.4mmHgと著明高値であり,肺高血圧症(PH)の診断。抗核抗体5120倍,抗セントロメア抗体陽性。嚥下困難と顔面,頚部,前胸部の毛細血管拡張,両前腕,右腰部に皮下石灰沈着があり,PHを伴ったCREST症候群と診断。肺線維症はないが,肺拡散能は低下し,酸素吸入療法等の対症療法に不応で,生命予後は不良と思われる。自験例は皮膚症状が先行していたが ...
KUBOTA, Yumiko +2 more
openaire +1 more source
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

