Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Pathological and Biochemical Studies of Mucopolysaccharidosis Type IIIB (Sanfilippo Syndrome Type B) in Juvenile Emus ( Dromaius novaehollandiae )

10 Apr 2014

Abstract excerpt

Mucopolysaccharidosis (MPS) type IIIB was diagnosed in 14 juvenile emus (Dromaius novaehollandiae), ages 3 weeks to 6 months, based on pathological and biochemical analyses. The animals had a history of neurological signs or sudden death; one of the birds with neurological signs and 3 others experienced acute hemoabdomen. Histopathologically, neuronal swelling and vacuolation in the cerebrum, cerebellum,...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cellular transport and secretion
Share to Complement system in diseases
Share to Lysosomal Storage Disorders Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 24723233
DOI: 10.1177/0300985814529314

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Pathological and Biochemical Studies of Mucopolysaccharidosis Type IIIB (Sanfilippo Syndrome Type B) in Juvenile Emus ( Dromaius novaehollandiae )PMID 24723233Read ↗

Mucopolysaccharidosis IIIB (Sanfilippo syndrome B) in a commercial emu (Dromaius novaehollandiae) flock.Semantic proximity Read ↗

Molecular basis of mucopolysaccharidosis type IIIB in emu (Dromaius novaehollandiae): an avian model of Sanfilippo syndrome type B.Semantic proximity Read ↗

Mucopolysaccharidosis-like phenotype in feline Sandhoff disease and partial correction after AAV gene therapy.Semantic proximity Read ↗

Zebrafish models of Mucopolysaccharidosis IIIA, IIIB, and IIIC show hyperactivity, neuroinflammation and changes in oligodendrocyte cell stateSemantic proximity Read ↗

Mapping Sanfilippo Syndrome: A Multisystem Clinicopathological AutopsySemantic proximity Read ↗

Lysosomal storage disease in two presumed-related springboks (Antidorcas marsupialis).Semantic proximity Read ↗

Mucopolysaccharidosis type VII in a German Shepherd Dog.Semantic proximity Read ↗

Pathogenesis of Morquio A syndrome: an autopsied case reveals systemic storage disorder.Semantic proximity Read ↗

Review of the principal diseases affecting cultured meagre (Argyrosomus regius)Semantic proximity Read ↗

A pathogenic HEXA missense variant in wild boars with Tay-Sachs disease.Semantic proximity Read ↗

Prevalence of mucopolysaccharidosis type VI mutations in Siamese cats.Semantic proximity Read ↗

[Clinical and molecular characteristics of a child with juvenile Sandhoff disease].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.