N. Kumar

发表

Myelin protein zero mutation His39Pro: hereditary motor and sensory neuropathy with variable onset, hearing loss, restless legs and multiple sclerosis

J. Cunningham, W. Litchy, P. Dyck, 2006, Journal of Neurology, Neurosurgery & Psychiatry.

Comparison of haematological and biochemical changes between non-anaemic and anaemic primigravid women in a north Indian population to establish normative values

R. Sandhir, N. Kumar, A. Kumar, 2015, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Neuroimaging in Superficial Siderosis: An In-Depth Look

N. Kumar, Neeraj Kumar, 2010, American Journal of Neuroradiology.

The spectrum of neurologic disease associated with anti‐GM1 antibodies

L. Berg, R. Lovelace, T. Munsat, 1990, Neurology.

Hepatopulmonary syndrome.

N. Kumar, D. Rosha, G. Agrawal, 2008, The Journal of the Association of Physicians of India.

Review article on VKC associated with ocular complication.

N. Kumar, R. Sharma, Vikash srivistav, 2022 .

High-definition spectral domain optical coherence tomography in the evaluation of ataxia with visual impairment

J. Pulido, N. Kumar, 2009, British Journal of Ophthalmology.

Common variable immunodeficiency-associated myelitis

J. Hagan, N. Kumar, R. Abraham, 2008, Journal of Neurology.

Cerebral hemiatrophy with superficial siderosis and PLEDs due to a germ cell tumor of the basal ganglia

J. Parisi, S. Kotagal, N. Kumar, 2006, European journal of neurology.

Severe vitamin D deficiency in a patient treated for hepatitis B with tenofovir

M. Nelson, N. Kumar, M. Bower, 2012, International journal of STD & AIDS.

Herlyn-Werner-Wunderlich Syndrome with Degenerating Fibroid – Uncommon Presentation of a Rare Anomaly

N. Kumar, V. Indiran, P. Maduraimuthu, 2018 .

Hepatic Sarcoidosis: Clinico-pathological characterization of symptomatic cases.

S. Sarin, C. Bihari, A. Rastogi, 2015, Acta gastro-enterologica Belgica.

SUPERFICIAL SIDEROSIS AND CSF HYPOVOLEMIA: THE DEFECT (DURAL) IN THE LINK

B. Mokri, A. Rabinstein, J. Ahlskog, 2007, Neurology.

Superficial siderosis

D. Piepgras, J. Ahlskog, A. Cohen-Gadol, 2006, Neurology.

SPONTANEOUS TIBIALIS ANTERIOR TENDON RUPTURE: A RARE CAUSE OF FOOT DROP

C. Klein, N. Kumar, D. Rubin, 2007, Neurology.

Melarsoprol-associated multifocal inflammatory CNS illness in African trypanosomiasis

A. Windebank, C. Klein, N. Kumar, 2006, Neurology.

Rupture renal pelvicalyceal system during pregnancy

N. Kumar, R. Keriakos, S. Najia, 2005, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

HYPERMANGANESEMIA, HEREDITARY HEMORRHAGIC TELANGIECTASIA, BRAIN ABSCESS: THE HEPATIC CONNECTION

B. Boeve, P. Kamath, K. Swanson, 2008, Neurology.

The ‘red Ear Syndrome’ Revisited: Two Cases and a Review of Literature

J. Swanson, N. Kumar, 2004, Cephalalgia : an international journal of headache.

Sevoflurane in child with carpus callosum agenesis syndrome, a series of four cases

N. Kumar, 2014 .

Hydatid disease.

N. Kumar, J. Chhatwal, M. Verma, 1991, Indian pediatrics.

Diffuse cerebral atrophy, central sinus venous thrombosis, hypoplastic carpus callosum, ADHD and VDS in a child: anaesthetic implications

N. Kumar, 2014 .

Mutation in the ATP7A gene may not be responsible for hypocupraemia in copper deficiency myelopathy

J. Gross, N. Kumar, 2006, Postgraduate Medical Journal.

Celiac Disease Presenting a Vitamin B12 Deficiency Associated Reversible Hyperpigmentation

N. Kumar, Shyama, 2018 .

POLYRADICULOPATHY DUE TO METHOTREXATE-INDUCED EBV-ASSOCIATED LYMPHOPROLIFERATIVE DISORDER

D. Steensma, H. Luthra, P. Sandroni, 2008, Neurology.