A study of histopathologic spectrum of nodular hidradenoma
BN Nandeesh, T Rajalakshmi - The American Journal of …, 2012 - journals.lww.com
Background: Hidradenomas are rare benign adnexal neoplasms that encompass a
morphological gamut with a range of differentiation. As a consequence, there is a great …
morphological gamut with a range of differentiation. As a consequence, there is a great …
[HTML][HTML] Psammomatoid juvenile ossifying fibroma: report of three cases with a review of literature
S Rao, BN Nandeesh, A Arivazhagan… - Journal of Pediatric …, 2017 - journals.lww.com
Psammomatoid juvenile ossifying fibroma (PJOF), a variant of juvenile ossifying fibroma
(JOF), is a locally aggressive neoplasm of the children and young adults. This entity has …
(JOF), is a locally aggressive neoplasm of the children and young adults. This entity has …
LIN28A, a sensitive immunohistochemical marker for Embryonal Tumor with Multilayered Rosettes (ETMR), is also positive in a subset of Atypical Teratoid/Rhabdoid …
S Rao, RT Rajeswarie, T Chickabasaviah Yasha… - Child's Nervous …, 2017 - Springer
Introduction CNS embryonal tumors comprise a group of highly malignant neoplasms with a
wide spectrum of histomorphological entities that includes Medulloblastoma (MB), Atypical …
wide spectrum of histomorphological entities that includes Medulloblastoma (MB), Atypical …
Neuromuscular disease genetics in under-represented populations: increasing data diversity
LA Wilson, WL Macken, LD Perry, CJ Record… - Brain, 2023 - academic.oup.com
Neuromuscular diseases (NMDs) affect∼ 15 million people globally. In high income settings
DNA-based diagnosis has transformed care pathways and led to gene-specific therapies …
DNA-based diagnosis has transformed care pathways and led to gene-specific therapies …
[HTML][HTML] Brain and spinal cord lesions in leprosy: A magnetic resonance imaging–based study
K Polavarapu, V Preethish-Kumar… - The American Journal …, 2019 - ncbi.nlm.nih.gov
Neurotropism and infiltration by Mycobacterium leprae of peripheral nerves causing
neuropathy are well established, but reports of central nervous system (CNS) damage are …
neuropathy are well established, but reports of central nervous system (CNS) damage are …
Intracranial fungal granuloma: a single-institute study of 90 cases over 18 years
A Mishra, AR Prabhuraj, DP Shukla, BN Nandeesh… - Neurosurgical …, 2019 - thejns.org
OBJECTIVE Intracranial fungal granuloma (IFG) remains an uncommon entity. The authors
report a single-institute study of 90 cases of IFG, which is the largest study until now …
report a single-institute study of 90 cases of IFG, which is the largest study until now …
A simple algorithmic approach using histology and immunohistochemistry for the current classification of adult diffuse glioma in a resource-limited set-up
RT Rajeswarie, S Rao, BN Nandeesh… - Journal of Clinical …, 2018 - jcp.bmj.com
Aims The WHO 2016 classification of diffuse gliomas combines histological and molecular
parameters for diagnosis. However, in view of cost constraints for molecular testing, an …
parameters for diagnosis. However, in view of cost constraints for molecular testing, an …
Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report
BN Nandeesh, PS Bindu, G Narayanappa… - …, 2020 - Wiley Online Library
Stroke is a major cause of mortality and morbidity with a wide variety of etiological risk
factors. Cerebral small vessel disease (SVD) is an important cause of stroke in the young …
factors. Cerebral small vessel disease (SVD) is an important cause of stroke in the young …
Childhood-Onset Myopathy With Preserved Ambulation Caused by a Recurrent ADSSL1 Missense Variant
D Baskar, K Polavarapu, V Preethish-Kumar… - Neurology …, 2024 - AAN Enterprises
Background and Objectives Distal myopathies are a heterogeneous group of primary
muscle disorders with recessive or dominant inheritance. ADSSL1 is a muscle-specific …
muscle disorders with recessive or dominant inheritance. ADSSL1 is a muscle-specific …
Novel variants broaden the phenotypic spectrum of PLEKHG5‐associated neuropathies
Background and purpose Pathogenic variants in PLEKHG5 have been reported to date to
be causative in three unrelated families with autosomal recessive intermediate Charcot …
be causative in three unrelated families with autosomal recessive intermediate Charcot …