Dr. Prabhudev M Hiremath MD 🧠
@Neuroptimist23
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Assistant Professor of Neurology & Pediatric Neurology at Ramaiah Hospital. Alumnus #PGIChandigarh. Neuro -therapeutics/genetics/immunology/rehabilitation.
Bengaluru,Karnataka.
Joined June 2019
Such an amazing experience I had while winning the #Karnataka Neurology quiz at #Tumakuru. Bright weekend. #KNACON 2024. #Medtwitter
#Neurology
#Neuroscience
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Almost a month, @CareMagicpin is still looking into the matter. Such a greedy and unethical bunch of people running the show.
@Neuroptimist23 Our team is looking into this. Please give us some time to get this checked & we’ll be back with an update soon!
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Just the quality of road even in suburbs.
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I honestly feel in a country like India, work-life balance will not take you far in life. Atleast till 45 we have to slog and sacrifice. PS: It’s my personal opinion and not speaking as a doctor here.
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A large number of neurological disorders are either genetic or Immune mediated.
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Dear Neurology/Pediatric Neurology friends ( only from India) on X, kindly go through the survey. I am sure you won’t regret it. Subject : Genetic Testing Practices Among Clinical Neurologists in India. #Neurology
https://t.co/URG0GhJnwg
survey.zohopublic.in
Your response would be greatly appreciated.
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It’s humbling experience to see a patient who was once shown at my alma mater.
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Hello, how much more time. Can you please get back?
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I am sensing this will pave a way to treat many incurable diseases.
2024 #NobelPrize laureate in chemistry David Baker has succeeded with the almost impossible feat of building entirely new kinds of proteins. In recent years, one incredible protein creation after the other has emerged from Baker’s laboratory. They range from new nanomaterials
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13Y/ M, ID, microcephaly, UMN facial weakness and spasticity. Any takers? @aditya_gan3500 @NeuroJediMaster @Shridha98131755 @SikandarAdwani
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30Y/M. Presented with giddiness. Newly detected hypertension.
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It made my day.
Huntington's disease has been successfully treated for the first time, doctors tell BBC
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Very interesting case. Diagnosed by another Neurologist. 6Y/F came for seeking second opinion. She was evaluated for CMT. Last year I had a 23Y/M who presented like typical SMA. Evaluated by MLPA first. Later whole exome revealed the same mutation. One case presented like
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Male child with infantile spasms. MRI s/o Cortical atrophy. Metabolic causes ruled out. MAST3 is a rare entity. First time I am seeing. I need to confirm this anyway. Anybody has seen this before?
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