: Intraorbital paragangliomas are rare. A case of intraorbital paraganglioma with extension
to the middle cranial fossa is reported. Progressive throbbing, hemicranial headaches, …

Merosin-deficient congenital muscular dystrophy is an autosomal recessive disease that
can manifest differently in different ethnic groups. This often presents as a floppy infant, and …

Cardiomyopathy is an important manifestation of several inborn errors of metabolism, 1 and
at times is the presenting problem in such disorders. 2 We report an infant boy who was …

Results A large majority of the autopsied cases were below 10 yr of age, the youngest
patient being li yr old. The duration of illness varied from l-16 days. Nearly half the patients …

… A few selected parts were reprocessed from the paraffin blocks according to the method
of Vasudev Rao, et al., ~6 for cutting semithin paraffin sections for better delineation of the …

A 45-year-old diabetic man presented with an episodic history of painless gross hematuria.
He had had no previous urinary symptoms or any other medical problems. His physical …

A case of multiple sclerosis in association with an oligodendroglioma is presented. The
aetiopathogenesis is briefly discussed. The unusual features were the clinically silent multiple …

There are very few recorded instances of brain tumors with ipsilateral secondary brain
atrophy. All 10 cases in the literature are from Japan. We report a case of primary cerebral …

We report a detailed morphological, ultrastructural and immunochemical features of neuronal
pathology in a case of Alzheimer's disease. This is probably the first detailed study of an …

We report a case of a multicentric plasma cell (PC) variant of Castleman's disease (CD) in
association with interfollicular type of classic Hodgkin's disease (HD), both diseases identified …