Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Arina Madan"'
Publikováno v:
The Pan African Medical Journal, Vol 28, Iss 110 (2017)
Hereditary chronic pancreatitis associated with a mutation in the serine protease inhibitor, Kazal Type-1 (SPINK-1 gene) is extremely rare. The SPINK1 mutation results in trypsinogen activation which predisposes to chronic pancreatitis predominately
Externí odkaz:
https://doaj.org/article/a2ae91b88f8d4042a41f4e3d0fb505b1
Publikováno v:
Cureus. 14(11)
Overactive bladder (OAB) is experienced by more than half of patients with untreated Parkinson's disease. Treatment of overactive bladder in these patients has included antimuscarinic anticholinergics, raising concerns about the possibility of exacer
Publikováno v:
Journal of Neurology
Publikováno v:
Expert Opinion on Orphan Drugs. 6:625-634
Introduction: Levodopa induced dyskinesia (LID) is a common motor complication affecting almost 95% of patients after 15 years of levodopa therapy. Dyskinesia in Parkinson`s disease (PD) can be fun...
Publikováno v:
International Journal of Neuroscience. 127:1136-1149
This clinical review aims to evaluate lower urinary tract symptoms (LUTS) in Parkinson's disease (PD) patients and the current treatment options available for these symptoms in a neurology setting. The review also addresses when referral to urology i
Autor:
Arina Madan, Alice M Turner
Publikováno v:
Eur Respir J
The characteristics that predict progression to overt chronic obstructive pulmonary disease (COPD) in smokers without spirometric airflow obstruction are not clearly defined. We conducted a post hoc analysis of 849 current and former smokers (≽20 p
Publikováno v:
Pan African Medical Journal; Vol 28, No 1 (2017); 150
The Pan African Medical Journal
The Pan African Medical Journal
Hereditary chronic pancreatitis associated with a mutation in the serine protease inhibitor, Kazal Type-1 (SPINK-1 gene) is extremely rare. The SPINK1 mutation results in trypsinogen activation which predisposes to chronic pancreatitis predominately