Search Results

You are looking at 1 - 3 of 3 items for :

  • craniopharyngioma x
Clear All
Sarah Craus Department of Medicine, Faculty of Medicine and Surgery, University of Malta, Mater Dei Hospital, Msida, Malta
Department of Medicine, Mater Dei Hospital, Msida, Malta

Search for other papers by Sarah Craus in
Google Scholar
PubMed
Close
and
Mark Gruppetta Department of Medicine, Faculty of Medicine and Surgery, University of Malta, Mater Dei Hospital, Msida, Malta
Department of Medicine, Mater Dei Hospital, Msida, Malta

Search for other papers by Mark Gruppetta in
Google Scholar
PubMed
Close

Introduction Craniopharyngiomas are rare but challenging tumours. Despite being a serious condition, population-based epidemiological data on craniopharyngiomas are limited in other studies ( Bunin et al. 1998 , Haupt et al . 2006

Open access
Nele F Lenders Department of Endocrinology, St Vincent’s Hospital, Sydney, NSW, Australia
Garvan Institute of Medical Research, Sydney, NSW, Australia
St Vincent’s Clinical School, University of New South Wales, Sydney, NSW, Australia

Search for other papers by Nele F Lenders in
Google Scholar
PubMed
Close
,
Peter E Earls Department of Anatomical Pathology and Cytopathology, St Vincent’s Pathology, Sydney, NSW, Australia

Search for other papers by Peter E Earls in
Google Scholar
PubMed
Close
,
Warrick J Inder Department of Diabetes and Endocrinology, Princess Alexandra Hospital, Brisbane, QLD, Australia
Faculty of Medicine, the University of Queensland, Brisbane, QLD, Australia

Search for other papers by Warrick J Inder in
Google Scholar
PubMed
Close
, and
Ann I McCormack Department of Endocrinology, St Vincent’s Hospital, Sydney, NSW, Australia
Garvan Institute of Medical Research, Sydney, NSW, Australia
St Vincent’s Clinical School, University of New South Wales, Sydney, NSW, Australia

Search for other papers by Ann I McCormack in
Google Scholar
PubMed
Close

sella region such as craniopharyngiomas or meningiomas. The authors have chosen not to discuss the proposed nomenclature change from ‘pituitary adenoma’ to ‘PitNET’, as described in the WHO 2022 classification, as this is the subject of significant

Open access
Sandra Pekic School of Medicine, University of Belgrade, Belgrade, Serbia
Clinic for Endocrinology, Diabetes and Metabolic Diseases, University Clinical Center Belgrade, Belgrade, Serbia

Search for other papers by Sandra Pekic in
Google Scholar
PubMed
Close
,
Marko Stojanovic School of Medicine, University of Belgrade, Belgrade, Serbia
Clinic for Endocrinology, Diabetes and Metabolic Diseases, University Clinical Center Belgrade, Belgrade, Serbia

Search for other papers by Marko Stojanovic in
Google Scholar
PubMed
Close
, and
Vera Popovic School of Medicine, University of Belgrade, Belgrade, Serbia

Search for other papers by Vera Popovic in
Google Scholar
PubMed
Close

, papillary craniopharyngioma and is identified in corticotroph adenomas ( Gualtieri et al. 2021 ). Mutations in BRAF have a high occurrence rate in different cancers. So the same underlying genetic driver has different unknown roles in different cell types

Open access