Sebagaimana telah diketahui bahwa seiring dengan bertambahnya jumlah penduduk, maka kebutuhan akan air bersih yang harus terpenuhi juga besar. Tujuan dari penelitian ini adalah untuk : (1) menyelidiki besaran per kapita di Kota Bandar Lampung; (2) mengidentifikasi faktor-faktor berpengaruh terhadap (3) menghitung biaya konsumsi bersih; (4) Melakukan perbandingan hasil mengenai dilakukan sebelum...

A. Baltussen · C. H. Kindler ()) Department of Anesthesia, Kantonsspital, University Clinics Basel, 4031 Basel, Switzerland e-mail: [email protected] Tel.: +41-61-2657254 Fax: +41-61-2657320 Abstract Objective: The number of citations an article receives after its publication reflects its impact on the scientific community. Our purpose was to identify and examine the characteristics of the most ...

Poikiloderma vasculare atrophicans (PVA) is a rare variant of mycosis fungoides, and is characterized by generalized hyperkeratotic scaly papules in net-like, retiform, or zebra-like patterns. A 59-year-old Korean woman presented with asymptomatic, erythematous-to-violaceous, reticulated confluent papules on the trunk and extremities. Skin lesions were initially limited to both thighs 25 years ...

La epidermólisis bullosa (EB) es un grupo heterogéneo de trastornos hereditarios caracterizado por aumento la fragilidad mucocutánea. El objetivo del presente estudio describir las características clínicas y epidemiológicas los pacientes con EB atendidos en el Hospital Universitario Paz, centro referencia nacional para hereditaria. Estudio observacional, retrospectivo unicéntrico. Se incluyeron...

Introdução: A Epidermólise Bolhosa hereditária (EB) é uma doença rara, caracterizada por formações de bolhas na pele e nas mucosas que sofrem mínimos traumas ou aparecem espontaneamente. As principais divisões EB são Simples, Juncional, Distrófica a Síndrome Kindler. manifestações bucais geralmente encontradas nos pacientes com as no epitélio oral, microstomia, anquiloglossia, periondontal, hip...

shwaehman syndrome, next to cystic fibrosis, is the second cause of congenita! exocrine pancreatic insufficiency in children. it appears as steatorrhea, recurrent infections and hematologic abnormalities such as neutropenia, skeletal dysplasia and short stature. in this study, we reviewed 3 patients' histories. all of them showed cellular chemotaxic defect. one of them had been affected by neph...