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1.
Global Spine J ; 3(2): 69-74, 2013 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24436854

RESUMO

The purpose of this article is to quantify changes in thickness of the ligamentum flavum (LF) associated with motion of the cervical spine and to compare the thickness of the LF at each cervical level using kinetic magnetic resonance imaging (kMRI). Two hundred fifty-seven symptomatic patients (129 men; 128 women) underwent kMRI in neutral, flexion, and extension positions. Midsagittal images were digitally marked and electronically analyzed by spine surgeons. Thickness of LF in the cervical region from C2-3 to C7-T1 was measured in all three positions. LF at C7-T1 was significantly thicker than C2-3 to C6-7 in neutral, flexion, and extension positions (p < 0.05). LF was significantly thicker in extension than in flexion at C3-4 to C6-7. LF thickness increases with extension and decreases with flexion. LF is uniquely thick at C6-7 and at C7-T1 in the extension position, which may predispose these levels to cord compression syndromes and associated neuropathies.

2.
Hautarzt ; 45(6): 378-84, 1994 Jun.
Artigo em Alemão | MEDLINE | ID: mdl-7520891

RESUMO

We report on an 11-year-old female patient with anhidrotic ectodermal dysplasia (AED) showing the following characteristics: (1) reduced number of hair follicles and incomplete formation of sweat glands; (2) disturbed hair growth with shortening of anagen and anhidrosis; (3) disturbed cytokeratin expression pattern of CK 13, 14, 19 (follicular epithelium) and of CK 18 (eccrine sweat glands); (4) reduction of cystine and increase in sulphonic cysteine acid. Thus, we demonstrated pathological differentiation on the immunomorphological and on the biochemical level, leading to disturbed keratinization that could be visualized by transmission and scanning electron microscopical studies of the hair shafts. According to these findings AED is a developmental defect that involves not only incomplete formation of hair follicles and sweat glands but also a disordered differentiation and follicular keratinization with disturbed cytokeratin pattern and pathological amino acid composition of the terminal hairs produced.


Assuntos
Diferenciação Celular/genética , Displasia Ectodérmica/genética , Doenças do Cabelo/genética , Queratinas/genética , Doenças das Glândulas Sudoríparas/genética , Anticorpos Monoclonais , Criança , Displasia Ectodérmica/patologia , Feminino , Cabelo/patologia , Doenças do Cabelo/patologia , Humanos , Técnicas Imunoenzimáticas , Microscopia Eletrônica de Varredura , Couro Cabeludo/patologia , Doenças das Glândulas Sudoríparas/patologia , Glândulas Sudoríparas/patologia , Anormalidades Dentárias/genética , Anormalidades Dentárias/patologia
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