Graeme Eisenhofer
Overview
Explore the profile of Graeme Eisenhofer including associated specialties, affiliations and a list of published articles.
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Articles
341
Citations
9494
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Recent Articles
1.
Richter S, Pacak K, Kunst H, Januszewicz A, Nolting S, Remde H, et al.
Eur J Endocrinol
. 2024 Sep;
191(4):389-398.
PMID: 39303070
Objective: Head-neck paragangliomas (HNPGLs) are rare tumors with approximately half arising due to germline pathogenic variants (PVs) in succinate dehydrogenase genes (SDHx). Patients with HNPGL have heterogeneous propensity to recur...
2.
Monteagudo M, Calsina B, Salazar-Hidalgo M, Martinez-Montes A, Pineiro-Yanez E, Caleiras E, et al.
Best Pract Res Clin Endocrinol Metab
. 2024 Sep;
38(6):101931.
PMID: 39218714
Pheochromocytomas and paragangliomas are rare neuroendocrine tumours. Around 20-25 % of patients develop metastases, for which there is an urgent need of prognostic markers and therapeutic stratification strategies. The presence...
3.
Hendriks A, Burns C, Fleming B, Harper I, Hook E, Armstrong R, et al.
J Clin Endocrinol Metab
. 2024 Aug;
110(3):855-862.
PMID: 39215571
Catecholamine-producing tumors of childhood include neuroblastic tumors, phaeochromocytoma, and paraganglioma (PPGL). PPGL and neuroblastic tumors can arise in similar anatomical locations and clinical presentations can overlap, resulting in diagnostic challenges....
4.
Casey R, Hendriks E, Deal C, Waguespack S, Wiegering V, Redlich A, et al.
Nat Rev Endocrinol
. 2024 Aug;
20(12):760.
PMID: 39191988
No abstract available.
5.
Casey R, Hendriks E, Deal C, Waguespack S, Wiegering V, Redlich A, et al.
Nat Rev Endocrinol
. 2024 Aug;
20(12):729-748.
PMID: 39147856
Phaeochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumours that arise not only in adulthood but also in childhood and adolescence. Up to 70-80% of childhood PPGL are hereditary, accounting for...
6.
Gebhardt M, Kunath C, Frobel D, Funk A, Peitzsch M, Nolting S, et al.
J Endocr Soc
. 2024 Aug;
8(9):bvae142.
PMID: 39145115
Background: Carriers of germline pathogenic variants (PVs) in succinate dehydrogenase genes () are at risk of developing tumors, including paragangliomas, gastrointestinal stromal tumors, and renal cell carcinomas. Early tumor detection...
7.
Li M, Zhang J, Pang Y, He Y, Shen Y, Wang J, et al.
Int J Surg
. 2024 Aug;
111(1):913-919.
PMID: 39093877
Background: Perioperative management to maintain intraoperative haemodynamic stability is crucial during surgical treatment of pheochromocytomas and paragangliomas (PPGLs). Although ~70% of PPGLs carry pathogenic variants (PVs) in susceptibility genes, whether...
8.
Pang Y, Zhang J, Jiang J, Pamporaki C, Li M, Bechmann N, et al.
Clin Endocrinol (Oxf)
. 2024 Apr;
101(3):234-242.
PMID: 38606576
Objective: Paragangliomas of the urinary bladder (UBPGLs) are rare neuroendocrine tumours and pose a diagnostic and surgical challenge. It remains unclear what factors contribute to a timely presurgical diagnosis. The...
9.
Knuchel R, Erlic Z, Gruber S, Amar L, Larsen C, Gimenez-Roqueplo A, et al.
Front Endocrinol (Lausanne)
. 2024 Apr;
15:1370525.
PMID: 38596218
Introduction: Endocrine hypertension (EHT) due to pheochromocytoma/paraganglioma (PPGL), Cushing's syndrome (CS), or primary aldosteronism (PA) is linked to a variety of metabolic alterations and comorbidities. Accordingly, patients with EHT and...
10.
Fuld S, Constantinescu G, Pamporaki C, Peitzsch M, Schulze M, Yang J, et al.
J Appl Lab Med
. 2024 Mar;
9(4):752-766.
PMID: 38532521
Background: Measurements of aldosterone by mass spectrometry are more accurate and less prone to interferences than immunoassay measurements, and may produce a more accurate aldosterone:renin ratio (ARR) when screening for...