Search Results - "K, Thiruvarutchelvan"

Limb Myokymia in Guillain-Barré Syndrome by Kuttiappan, Gunasekaran, Sivakumar, S, Thiruvarutchelvan, K

“…Focal myokymia involving facial muscles is noted in intramedullary brainstem lesions such as multiple sclerosis, pontine glioma, posterior fossa tumor,…”
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Two siblings with atypical pantothenate-kinase-associated neurodegeneration by K, Gunasekaran, S, Sivakumar, K, Thiruvarutchelvan

“…{Figure 5} PKAN is a rare autosomal recessive disorder caused by mutation in the pantothenate kinase 2 (PANK2) gene located in chromosome 20. Abnormal iron…”
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Parry-Romberg syndrome (progressive hemifacial atrophy) with spasmodic dysphonia--a rare association by Mugundhan, K, Selvakumar, C J, Gunasekaran, K, Thiruvarutchelvan, K, Sivakumar, S, Anguraj, M, Arun, S

“…Parry-Romberg syndrome is a rare clinical entity characterised by progressive hemifacial atrophy with appearance of 'saber'. Various neurological and…”
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Congenital crocodile tears with Duane's syndrome--congenital cranial dysinnervation syndrome by Mugundhan, K, Thiruvarutchelvan, K, Sivakumar, S

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Epidermal nevus syndrome--a neuro-cutaneous marker by Mugundhan, K, Thiruvarutchelvan, K, Sivakumar, S

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Cerebral Venous Thrombosis in Papillary Carcinoma Thyroid by Krishnan, Mugundhan, N, Balamurugan, K, Thiruvarutchelvan, S, Sivakumar

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Crossed Aphasia by Krishnan, Mugundhan, N, Balamurugan, K, Thiruvarutchelvan, S, Sivakumar

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Wernicke's Encephalopathy: A Rare Complication of Hyperemesis Gravidarum by Krishnan, Mugundhan, N, Balamurugan, K, Thiruvarutchelvan, S, Sivakumar

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Carcinoma Prostate Presenting as Multiple Cranial Nerve Palsy by Mugundhan, Krishnan, Arasi, K V, Balamurugan, N, Chandrasekaran, P, Thiruvarutchelvan, K, Sivakumar, S

“…Metastatic prostatic carcinoma commonly involves bones and extra pelvic lymph nodes. CNS involvement is unusual and particularly the occurence of…”
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Familial episodic ataxia type II by Mugundhan, K, Thiruvarutchelvan, K, Sivakumar, S

“…The familial episodic ataxia type II is a rare, dominantly inherited disease characterized by episodes of ataxia of early onset, often with completely normal…”
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Isolated Sixth Cranial Nerve Palsy--An Uncommon Presenting Feature of Multiple Sclerosis by Mugundhan, K, Thiruvarutchelvan, Manikandan, D, Sivakumar, S

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