Aller au contenu principal
Profil bibliographique

Sreenath Thati Ganganna

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

11Publications signalées
54Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Neuroscience of respiration and sleepObstructive Sleep Apnea ResearchSleep and Wakefulness ResearchCerebral Palsy and Movement DisordersAdvanced Neuroimaging Techniques and Applications

Les publications récentes

Accès ouvert 2026 article OpenAlex

Human forebrain neural synchronization and entrainment to breathing during wakefulness, sleep, and external mechanical ventilation

Md Rakibul Mowla, Ariane E. Rhone, Sukhbinder Kumar, Christopher K. Kovach et autres

The ability of the forebrain to track and integrate respiratory signals, a process known as breathing interoception, is critical for detecting respiratory threats and ensuring survival, yet its neural mechanisms remain largely unknown. Using human intracranial recordings, we identified widespread synchronization between …

us, gb (code pays fourni par la source)

0 citations Nature Communications
Accès ouvert 2026 article OpenAlex

A motor thalamic site in humans that suppresses involuntary breathing without awareness

Sukhbinder Kumar, Ariane E. Rhone, Christopher K. Kovach, Md Rakibul Mowla et autres

This study identifies a focal site in the human motor thalamus where electrical stimulation suppresses involuntary, automatic breathing and induces apnea without awareness. Using intracranial recordings in pediatric and adult patients, we found that this effect localizes to the ventral anterior/ventral lateral …

us, gb (code pays fourni par la source)

0 citations Journal of Neurophysiology
Accès ouvert 2024 article OpenAlex

Recurrent super-refractory status epilepticus and stroke like episode in a patient with Behr syndrome secondary to biallelic variants in OPA1 gene

Spoorthi Jagadish, Amy R. U. L. Calhoun, Sreenath Thati Ganganna

Behr syndrome is associated with compound heterozygous dysfunction in OPA1 gene and typically presents with a constellation of visual impairment due to early onset optic atrophy, cerebellar ataxia, peripheral neuropathy, deafness, and gastrointestinal motility problems. Our patient with biallelic variants in OPA1 …

us (code pays fourni par la source)

2 citations Epilepsy & Behavior Reports
Accès ouvert 2021 article OpenAlex

Atypical presentation of SLC30A10 gene mutation with hypermanganesemia, seizures and polycythemia

Spoorthi Jagadish, Lillian Howard, Sreenath Thati Ganganna

Manganese is an essential element that is ubiquitously present in our diet and water supply. It is a cofactor for several critical physiological processes. Elevated blood levels of Manganese secondary to SLC30A10 gene mutation presents distinctly with dystonia, polycythemia, chronic liver disease …

us (code pays fourni par la source)

8 citations Epilepsy & Behavior Reports

BNTIC News n’est pas le producteur de ces données. Les publications sont interrogées à la demande dans Crossref, OpenAIRE, DOAJ, Europe PMC, HAL, DataCite, AfricArXiv, ROR et la Banque mondiale, sans clé d’accès. OpenAlex reste optionnel. Aucun service payant n’est nécessaire et aucune donnée externe n’est enregistrée en base. Consulter les sources et leurs limites.