OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Multiple endocrine neoplasia type 4 (MEN4): a thorough update on the latest and least known men syndrome
Rosaria Maddalena Ruggeri, Elio Benevento, Federica de Cicco, et al.
Endocrine (2023) Vol. 82, Iss. 3, pp. 480-490
Closed Access | Times Cited: 15
Rosaria Maddalena Ruggeri, Elio Benevento, Federica de Cicco, et al.
Endocrine (2023) Vol. 82, Iss. 3, pp. 480-490
Closed Access | Times Cited: 15
Showing 15 citing articles:
Association of primary hyperparathyroidism with pituitary adenoma and management issues
Liza Das, Pinaki Dutta
Best Practice & Research Clinical Endocrinology & Metabolism (2025), pp. 101978-101978
Closed Access | Times Cited: 1
Liza Das, Pinaki Dutta
Best Practice & Research Clinical Endocrinology & Metabolism (2025), pp. 101978-101978
Closed Access | Times Cited: 1
Circulating non-coding RNA biomarkers of endocrine tumours
Henriett Butz, Attila Patócs, Péter Igaz
Nature Reviews Endocrinology (2024) Vol. 20, Iss. 10, pp. 600-614
Closed Access | Times Cited: 7
Henriett Butz, Attila Patócs, Péter Igaz
Nature Reviews Endocrinology (2024) Vol. 20, Iss. 10, pp. 600-614
Closed Access | Times Cited: 7
Neuroendocrine Tumors: Germline Genetics and Hereditary Syndromes
E Lauricella, Nada Chaoul, Gabriella D’Angelo, et al.
Current Treatment Options in Oncology (2025)
Closed Access
E Lauricella, Nada Chaoul, Gabriella D’Angelo, et al.
Current Treatment Options in Oncology (2025)
Closed Access
Perforated peptic ulcer disease as the initial presentation of previously unknown multiple myeloma and sickle cell anaemia
Matthew Gowell, A Morrow
BMJ Case Reports (2025) Vol. 18, Iss. 2, pp. e261990-e261990
Closed Access
Matthew Gowell, A Morrow
BMJ Case Reports (2025) Vol. 18, Iss. 2, pp. e261990-e261990
Closed Access
Ectopic GHRH production: revisiting a rare cause of acromegaly
Matheo Augusto Morandi Stumpf, Nathalie Oliveira de Santana, Márcio Carlos Machado, et al.
Reviews in Endocrine and Metabolic Disorders (2025)
Closed Access
Matheo Augusto Morandi Stumpf, Nathalie Oliveira de Santana, Márcio Carlos Machado, et al.
Reviews in Endocrine and Metabolic Disorders (2025)
Closed Access
An Updated Perspective of the Clinical Features and Parathyroidectomy Impact in Primary Hyperparathyroidism Amid Multiple Endocrine Neoplasia Type 1 (MEN1): Focus on Bone Health
Ana-Maria Gheorghe, Mihaela Stanciu, Ioana Codruta Lebada, et al.
Journal of Clinical Medicine (2025) Vol. 14, Iss. 9, pp. 3113-3113
Open Access
Ana-Maria Gheorghe, Mihaela Stanciu, Ioana Codruta Lebada, et al.
Journal of Clinical Medicine (2025) Vol. 14, Iss. 9, pp. 3113-3113
Open Access
MEN4: l’ultima e meno nota sindrome MEN
Franco Fedeli, Natalia S. Pellegata
L Endocrinologo (2025)
Closed Access
Franco Fedeli, Natalia S. Pellegata
L Endocrinologo (2025)
Closed Access
Unlocking the Genetic Secrets of Acromegaly: Exploring the Role of Genetics in a Rare Disorder
Ioana Balinisteanu, Lavinia Caba, Andreea Florea, et al.
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 8, pp. 9093-9121
Open Access | Times Cited: 3
Ioana Balinisteanu, Lavinia Caba, Andreea Florea, et al.
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 8, pp. 9093-9121
Open Access | Times Cited: 3
Genetic Testing in Hereditary Pituitary Tumors
Gamze Akkuş, Márta Korbonits
Archives of Medical Research (2023) Vol. 54, Iss. 8, pp. 102920-102920
Closed Access | Times Cited: 5
Gamze Akkuş, Márta Korbonits
Archives of Medical Research (2023) Vol. 54, Iss. 8, pp. 102920-102920
Closed Access | Times Cited: 5
Tumorprädisposition in der Endokrinologie – von MEN bis FIPA
Lina Jegodzinski, Judith Gebauer
DMW - Deutsche Medizinische Wochenschrift (2024) Vol. 149, Iss. 06, pp. 283-289
Closed Access | Times Cited: 1
Lina Jegodzinski, Judith Gebauer
DMW - Deutsche Medizinische Wochenschrift (2024) Vol. 149, Iss. 06, pp. 283-289
Closed Access | Times Cited: 1
Genotype and clinical phenotype characteristics of MAX germline mutation–associated pheochromocytoma/paraganglioma syndrome
Bijun Lian, Jun Lü, Xu-Dong Fang, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 1
Bijun Lian, Jun Lü, Xu-Dong Fang, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 1
Insulinoma: A Novel Presentation of MEN4
Hye Jeong Han, Jacob Moalem, Angela Shih, et al.
AACE Clinical Case Reports (2024)
Closed Access | Times Cited: 1
Hye Jeong Han, Jacob Moalem, Angela Shih, et al.
AACE Clinical Case Reports (2024)
Closed Access | Times Cited: 1
Neoplasia endocrina múltiple
Eider Pascual‐Corrales, Marta Araujo‐Castro, A.E. Ortiz-Flores, et al.
Medicine - Programa de Formación Médica Continuada Acreditado (2024) Vol. 14, Iss. 13, pp. 738-749
Closed Access
Eider Pascual‐Corrales, Marta Araujo‐Castro, A.E. Ortiz-Flores, et al.
Medicine - Programa de Formación Médica Continuada Acreditado (2024) Vol. 14, Iss. 13, pp. 738-749
Closed Access
Appendiceal NET in an 18-year-old woman, the youngest case of MEN4 with neuroendocrine manifestation: case report and review of the current literature
Filippo Maria Bolamperti, Francesca Giusti, Francesca Marini, et al.
International Journal of Bone Fragility (2024) Vol. 3, Iss. 3, pp. 112-116
Closed Access
Filippo Maria Bolamperti, Francesca Giusti, Francesca Marini, et al.
International Journal of Bone Fragility (2024) Vol. 3, Iss. 3, pp. 112-116
Closed Access
Unveiling a rare endocrine puzzle: A case of CDKN1B mutation-associated MEN4 syndrome
Sunil Epuri, Dudi Nikitha, Kalyan Ram Uppaluri, et al.
Gene Reports (2024) Vol. 37, pp. 102089-102089
Closed Access
Sunil Epuri, Dudi Nikitha, Kalyan Ram Uppaluri, et al.
Gene Reports (2024) Vol. 37, pp. 102089-102089
Closed Access
