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Olfaction differentiates parkin disease from early-onset parkinsonism and Parkinson disease

Neurology, 2004-04, Vol.62 (7), p.1224-1226

2004

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Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation

Neurology, 2005-01, Vol.64 (1), p.134-136

2005

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Histopathology of VGKC antibody-associated limbic encephalitis

Neurology, 2009-05, Vol.72 (19), p.1703-1705

2009

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Progression of nigrostriatal dysfunction in a parkin kindred: an [18F]dopa PET and clinical study

Brain (London, England : 1878), 2002-10, Vol.125 (10), p.2248-2256

2002

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Safety of research bronchoscopy, biopsy and bronchoalveolar lavage in asthma

The European respiratory journal, 2004-09, Vol.24 (3), p.375-377

2004

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Basophils, eosinophils, and mast cells in atopic and nonatopic asthma and in late-phase allergic reactions in the lung and skin

Journal of allergy and clinical immunology, 2000-01, Vol.105 (1), p.99-107

2000

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Cyclosporin A, apoptosis of BAL T-cells and expression of Bcl-2 in asthmatics

The European respiratory journal, 2003-08, Vol.22 (2), p.207-212

2003

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Parkin disease: a phenotypic study of a large case series

Brain (London, England : 1878), 2003-06, Vol.126 (6), p.1279-1292

2003

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Attenuation of the allergen-induced late asthmatic reaction by cyclosporin A is associated with inhibition of bronchial eosinophils, interleukin-5, granulocyte macrophage colony-stimulating factor, and eotaxin

American journal of respiratory and critical care medicine, 2000-10, Vol.162 (4), p.1377-1382

2000

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Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study

Brain (London, England : 1878), 2002, Vol.125 (Pt 1), p.44-57

2002

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A Comparative Biometric Study on Indian Shad Gudusia chapra (Hamilton, 1822) Collected from Two Different River Ecosystems

Ambient science, 2022-12, Vol.9/10 (3/01 & 02), p.59-63

2022

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Malignant Infantile Osteopetrosis with Bone Marrow Involvement

Kathmandu University medical journal, 2022-03, Vol.20 (1), p.107-110

2022

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Malignant Infantile Osteopetrosis with Bone Marrow Involvement

Kathmandu University medical journal, 2022-01, Vol.20 (77), p.107-110

2022

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Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

Brain (London, England : 1878), 2005-12, Vol.128 (12), p.2786-2796

2005

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Recent Advances in the Treatment of Delusional Disorder

Canadian journal of psychiatry, 2006-02, Vol.51 (2), p.114-119

2006

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Striatal and cortical pre‐ and postsynaptic dopaminergic dysfunction in sporadic parkin‐linked parkinsonism

Brain (London, England : 1878), 2004-06, Vol.127 (6), p.1332-1342

2004

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Autosomal recessive, DYT2-like primary torsion dystonia: a new family

Neurology, 2003-12, Vol.61 (12), p.1801-1803

2003

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Parkinsonism and nigrostriatal dysfunction are associated with spinocerebellar ataxia type 6 (SCA6)

Movement disorders, 2005-09, Vol.20 (9), p.1115-1119

2005

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IS THERE ANY SIGNIFICANT IMPACT OF TWO DIFFERENT BIO-COMPATIBLE COATED CARDIOPULMONARY BYPASS CIRCUITS ON CIRCULATING PLATELET DROP

Biological and Clinical Sciences Research Journal, 2023-10, Vol.2023 (1), p.533

2023

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Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow-up over 10 years

Movement disorders, 2005-04, Vol.20 (4), p.479-484

2005

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Nigral degeneration and striatal dopaminergic dysfunction in idiopathic and parkin-linked Parkinson's disease

Movement disorders, 2006-03, Vol.21 (3), p.299-305

2006

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Prader-Willi and Angelman syndromes: update on genetic mechanisms and diagnostic complexities

Current opinion in neurology, 1999-04, Vol.12 (2), p.149-154

1999

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Enhanced Cyclooxygenase-2 Expression in Sporadic and Familial Adenomatous Polyposis of the Human Colon

Scandinavian journal of gastroenterology, 2001, Vol.36 (8), p.865-869

K. N. M. Khan, J. L. Masferrer, B. M. Woerner, R. Soslow, A. T. Koki

2001

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Familial Parkinsonian (Parkinson’s Disease and early onset Parkinsonism): a genetic, clinical and 18F dopa PET

Khan, N L

2007

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Olfaction differentiates parkin disease from early-onset parkinsonism and Parkinson disease

Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation

Histopathology of VGKC antibody-associated limbic encephalitis

Progression of nigrostriatal dysfunction in a parkin kindred: an [18F]dopa PET and clinical study

Safety of research bronchoscopy, biopsy and bronchoalveolar lavage in asthma

Basophils, eosinophils, and mast cells in atopic and nonatopic asthma and in late-phase allergic reactions in the lung and skin

Cyclosporin A, apoptosis of BAL T-cells and expression of Bcl-2 in asthmatics

Parkin disease: a phenotypic study of a large case series

Attenuation of the allergen-induced late asthmatic reaction by cyclosporin A is associated with inhibition of bronchial eosinophils, interleukin-5, granulocyte macrophage colony-stimulating factor, and eotaxin

Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study

Phenotype, genotype, and worldwide genetic penetrance of LRRK2 -associated Parkinson's disease: a case-control study

A Comparative Biometric Study on Indian Shad Gudusia chapra (Hamilton, 1822) Collected from Two Different River Ecosystems

Malignant Infantile Osteopetrosis with Bone Marrow Involvement

Malignant Infantile Osteopetrosis with Bone Marrow Involvement

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

Recent Advances in the Treatment of Delusional Disorder

Striatal and cortical pre‐ and postsynaptic dopaminergic dysfunction in sporadic parkin‐linked parkinsonism

Autosomal recessive, DYT2-like primary torsion dystonia: a new family

Parkinsonism and nigrostriatal dysfunction are associated with spinocerebellar ataxia type 6 (SCA6)

IS THERE ANY SIGNIFICANT IMPACT OF TWO DIFFERENT BIO-COMPATIBLE COATED CARDIOPULMONARY BYPASS CIRCUITS ON CIRCULATING PLATELET DROP

Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow-up over 10 years

Nigral degeneration and striatal dopaminergic dysfunction in idiopathic and parkin-linked Parkinson's disease

Prader-Willi and Angelman syndromes: update on genetic mechanisms and diagnostic complexities

Enhanced Cyclooxygenase-2 Expression in Sporadic and Familial Adenomatous Polyposis of the Human Colon

Familial Parkinsonian (Parkinson’s Disease and early onset Parkinsonism): a genetic, clinical and 18F dopa PET

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