WordNet

an impairment of health or a condition of abnormal functioning
caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological

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Atypical association of ethmoidal encephalocele and hydrocephalus in an adult patient with Autosomal Dominant Osteopetrosis type I (ADO-I): a case report.

Rossini Z1, Castellani C2, Borsa S2, Carrabba G2, Locatelli M2, Di Cristofori A2.
World neurosurgery.World Neurosurg.2016 Feb 3. pii: S1878-8750(16)00158-3. doi: 10.1016/j.wneu.2016.01.070. [Epub ahead of print]
BACKGROUND: Osteopetroses are a heterogeneous group of heritable disorders characterized by increased bone density due to defective osteoclast-mediated bone resorption. The Autosomal Dominant Osteopetrosis type I (ADO-I) is defined by the presence of osteosclerosis involving mainly the skull bones,
PMID 26851742

Report of the European Respiratory Society/European Cystic Fibrosis Society task force on the care of adults with cystic fibrosis.

Elborn JS1, Bell SC2, Madge SL3, Burgel PR4, Castellani C5, Conway S6, De Rijcke K7, Dembski B8, Drevinek P9, Heijerman HG10, Innes JA11, Lindblad A12, Marshall B13, Olesen HV14, Reimann AL15, Solé A16, Viviani L17, Wagner TO18, Welte T19, Blasi F20.
The European respiratory journal.Eur Respir J.2016 Feb;47(2):420-8. doi: 10.1183/13993003.00592-2015. Epub 2015 Oct 9.
The improved survival in people with cystic fibrosis has led to an increasing number of patients reaching adulthood. This trend is likely to be maintained over the next decades, suggesting a need to increase the number of centres with expertise in the management of adult patients with cystic fibrosi
PMID 26453627

Assessment, Definition, and Classification of Lower Limb Ulcers in Systemic Sclerosis: A Challenge for the Rheumatologist.

Blagojevic J1, Piemonte G1, Benelli L1, Braschi F1, Fiori G1, Bartoli F1, Guiducci S1, Bellando Randone S1, Galluccio F1, Cometi L1, Castellani S1, Boddi M1, Moggi Pignone A1, Rasero L1, Epifani F1, Matucci-Cerinic M1.
The Journal of rheumatology.J Rheumatol.2016 Feb 1. pii: jrheum.150035. [Epub ahead of print]
OBJECTIVE: To evaluate pathogenesis and clinical features of lower limb ulcers in systemic sclerosis (SSc) and to propose a classification that could be used in clinical practice.METHODS: Charts of 60 patients with SSc who had lower limb cutaneous lesions were reviewed. All patients had videocapilla
PMID 26834223