Results 131 to 140 of about 38,110 (241)

Mandibular Brown Tumor Revealing Hyperparathyroidism in a Patient With Neurofibromatosis Type I: Case Report. [PDF]

Glob Pediatr Health, 2023
Kabila B, Beqqali B, Obilat S, Haddad SE, Allali N, Chat L.   +5 more
europepmc   +1 more source

Molecular profile of atypical Leydig cell tumours

Histopathology, Volume 88, Issue 3, Page 628-635, February 2026.
Copy number variations by themselves are not sufficient to discriminate between benign and potential malignant Leydig cell tumours (LCTs). Genomic instability was only detected in malignant and atypical cases, and not in any benign tumours. Currently, the presence of metastasis remains the only malignant criterion for LCTs.
Muhammad F.K. Choudhry, Diogo Caires, Yaser Gamallat, Asli Yilmaz, Fadi Brimo, Bob Argiropoulos, Tarek A. Bismar   +6 more
wiley   +1 more source

Neurofibromatosis Type I Presenting with Incomplete Ileal Volvulus in a Pediatric Patient. [PDF]

Am J Case Rep, 2023
Rivera Fernández RR, Cancel Artau KJ, Añeses Gonzalez CR, Correa Rivas MS, Cintron Diaz E, Ortiz Justiniano V, Lara Del Río J.   +6 more
europepmc   +1 more source

Healthcare Utilisation and Barriers and Facilitators of Healthcare Access for Young People With Intellectual Disability: A Systematic Review

Journal of Intellectual Disability Research, Volume 70, Issue 2, Page 130-161, February 2026.
ABSTRACT Background Young people with intellectual disability may exhibit poorer general health, higher mortality rates and greater limitations from physical or mental illnesses compared to the general population. It is important to understand how this may relate to healthcare utilisation, including factors influencing healthcare access for young ...
Felicia Kreps, Shalini Wijekulasuriya, Yvonne Zurynski, Rebecca Mitchell   +3 more
wiley   +1 more source

Occipital bone defect caused by neurofibromatosis type I: A case report. [PDF]

Medicine (Baltimore), 2023
Wang Y, Song S, Li Z, Zhao Y, Miao J, Wang Z.   +5 more
europepmc   +1 more source

Histoplasmosis mimicking a tumor of the thumb in a patient with neurofibromatosis type I: A case report and review of the literature. [PDF]

Clin Case Rep, 2023
Levine JM, Manivel J, Luna J.
europepmc   +1 more source

Spontaneous Vertebral Artery Arteriovenous Fistula with Neurofibromatosis Type I and Its Management with Covered Stent. [PDF]

Asian J Neurosurg, 2023
Diyora B, Purandare A, Devani K, Palave P.   +3 more
europepmc   +1 more source

Neurofibromatosis Type I in Childhood [PDF]

Archives of Neurology, 1998
openaire   +2 more sources

End-stage renal disease due to retroperitoneal fibrosis in neurofibromatosis type I. [PDF]

Intractable Rare Dis Res, 2023
Ramanzini LG, Camargo LFM, Caixeta TLO, Louzada RC, Frare JM.   +4 more
europepmc   +1 more source

[Von Recklinghausen's neurofibromatosis (neurofibromatosis type I)--a familial case report].

Medicinski pregled, 2001
Neurofibromatosis is a term used for two disorders: NF-1 and NF-2. NF-1 is Von Recklinghasusen's neurofibromatosis and comprises characteristic skin lesions (cafe au lait spots, intertriginous freckles, neurofibromatous skin tumors) and other congenital and hamartomatous bone, endocrine glands and central nervous system lesions. Its incidence is one in
S, Tasić, S, Stojanović, M, Poljacki, Z, Janjić, J, Jovanović-Privrodski   +4 more
openaire   +1 more source