hypertrichosis/phosphatase

O link é salvo na área de transferência

ArtigosTestes clínicosPatentes

Escolha o tipo de classificação

9 resultados

Hair growth-stimulating effects of cyclosporin A and FK506, potent immunosuppressants.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Cyclosporin A (CsA), a cyclic endecapeptide, is a T cell-specific immunosuppressant and is successfully used in the field of organ transplantation. Another T cell-specific immunosuppressant, FK506, a more recently discovered macrolide antibiotic, is effective against graft rejection at much lower

[Immunosuppression with cyclosporin after orthoptic liver transplant in pigs].

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

The immunosuppressive effect of cyclosporine A (CsA) was studied in six pigs that underwent orthotopic liver transplant (OLT). The drug was administered i.v. in low doses (1.5-4 mg/Kg-1/12 h-1) and associated with wide spectrum antibiotics. The mean survival of the animals was 23.4 +/- 11.2 days.

Congenital erythropoietic porphyria: a case report.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Congenital erythropoietic porphyria is a rare autosomal recessive disorder of heme synthesis resulting from deficiency of uroporphyrinogen III synthase (UROIIIS). It is the most severe porphyria. The clinical manifestations are markedly variable due to the different mutation in the UROIIIS gene. We

Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Cantú syndrome consists of hypertrichosis, osteochondrodysplasia, and cardiomegaly, and has been reported in 18 patients to date. We report an infant with Cantú syndrome. In addition to typical findings, he had relatively mild radiological and cardiological manifestations. Previously undescribed

New syndrome of simplified gyral pattern, micromelia, dysmorphic features and early death.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

We report two sisters with a new syndrome of simplified gyral pattern, normal head circumference at birth but with subsequent development of microcephaly, intractable seizures, and early death. Dysmorphic features included coarse face, hypertrichosis, short nose, paranasal widening, long philtrum,

Familial benign chronic intrahepatic cholestasis.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Three of four adult siblings in a family which was studied for three generations had clinical and/or laboratory signs of slowly progressive intrahepatic cholestasis. Slight hyperpigmentation, facial hypertrichosis, and hypothyroidism were seen in affected individuals who also had prolonged increase

Congenital erythropoietic porphyria: skeletal manifestations and effect of pamidronate treatment.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Congenital erythropoietic porphyria (CEP) is a rare disorder of heme biosynthesis. Skeletal abnormalities have been described in patients with this disease. We report a 25-year-old woman with osteodystrophy from CEP. On examination, mild hepatosplenomegaly, multiple hyperpigmented scars,

Prostaglandin induced cortical hyperostosis in neonates with cyanotic heart disease.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

OBJECTIVE To study the side effects of prolonged prostaglandin therapy especially hyperostosis and other musculoskeletal changes. METHODS Case files of the neonates, with cyanotic heart disease, who had received prostaglandin infusion from early days of life, were reviewed. Patients with periosteal

Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca2+-Activated K+ Channel SK3 Cause Zimmermann-Laband Syndrome.

Apenas usuários registrados podem traduzir artigos

Entrar Inscrever-se

Zimmermann-Laband syndrome (ZLS) is characterized by coarse facial features with gingival enlargement, intellectual disability (ID), hypertrichosis, and hypoplasia or aplasia of nails and terminal phalanges. De novo missense mutations in KCNH1 and KCNK4, encoding K⁺ channels, have been

Junte-se à nossa
página do facebook

Herbal & Natural Medicine

O mais completo banco de dados de ervas medicinais apoiado pela ciência

Funciona em 55 idiomas
Curas herbais apoiadas pela ciência
Reconhecimento de ervas por imagem
Mapa GPS interativo - marcar ervas no local (em breve)
Leia publicações científicas relacionadas à sua pesquisa
Pesquise ervas medicinais por seus efeitos
Organize seus interesses e mantenha-se atualizado com as notícias de pesquisa, testes clínicos e patentes

Digite um sintoma ou doença e leia sobre ervas que podem ajudar, digite uma erva e veja as doenças e sintomas contra os quais ela é usada.
* Todas as informações são baseadas em pesquisas científicas publicadas