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Profile of altered brain iron acquisition in restless legs syndrome
Profile of altered brain iron acquisition in restless legs syndrome
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Profile of altered brain iron acquisition in restless legs syndrome

CONNOR, James R ; PONNURU, Padmavathi ; WANG, Xin-Sheng ; PATTON, Stephanie M ; ALLEN, Richard P ; EARLEY, Christopher J

Brain (London, England : 1878), 2011-04, Vol.134 (Pt 4), p.959-968 [Periódico revisado por pares]

Oxford: Oxford University Press

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2
Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development
Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development
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Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development

Simpson, M.A. ; Hsu, R. ; Keir, L.S. ; Hao, J. ; Sivapalan, G. ; Ernst, L.M. ; Zackai, E.H. ; Al-Gazali, L.I. ; Hulskamp, G. ; Kingston, H.M. ; Prescott, T.E. ; Ion, A. ; Patton, M.A. ; Murday, V. ; George, A. ; Crosby, A.H.

American journal of human genetics, 2007-11, Vol.81 (5), p.906-912 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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3
The natural history of Noonan syndrome: a long-term follow-up study
The natural history of Noonan syndrome: a long-term follow-up study
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The natural history of Noonan syndrome: a long-term follow-up study

Shaw, A C ; Kalidas, K ; Crosby, A H ; Jeffery, S ; Patton, M A

Archives of disease in childhood, 2007-02, Vol.92 (2), p.128-132 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

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4
The accuracy of pedometer steps and time during walking in children
The accuracy of pedometer steps and time during walking in children
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The accuracy of pedometer steps and time during walking in children

BEETS, Michael W ; PATTON, Megan M ; EDWARDS, Stacey

Medicine and science in sports and exercise, 2005-03, Vol.37 (3), p.513-520 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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5
Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia
Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia
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Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia

Simpson, MA ; Scheuerle, A ; Hurst, J ; Patton, MA ; Stewart, H ; Crosby, AH

Clinical genetics, 2009-03, Vol.75 (3), p.271-276 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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6
The impact of steatosis on disease progression and early and sustained treatment response in chronic hepatitis C patients
The impact of steatosis on disease progression and early and sustained treatment response in chronic hepatitis C patients
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The impact of steatosis on disease progression and early and sustained treatment response in chronic hepatitis C patients

Patton, Heather M ; Patel, Keyur ; Behling, Cynthia ; Bylund, David ; Blatt, Lawrence M ; Vallée, Marc ; Heaton, Shanon ; Conrad, Andrew ; Pockros, Paul J ; McHutchison, John G

Journal of hepatology, 2004-03, Vol.40 (3), p.484-490 [Periódico revisado por pares]

Oxford: Elsevier B.V

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7
Robinow syndrome
Robinow syndrome
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Robinow syndrome

Patton, M A ; Afzal, A R

Journal of medical genetics, 2002-05, Vol.39 (5), p.305-310 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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8
Mitochondrial Ferritin in the Substantia Nigra in Restless Legs Syndrome
Mitochondrial Ferritin in the Substantia Nigra in Restless Legs Syndrome
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Mitochondrial Ferritin in the Substantia Nigra in Restless Legs Syndrome

Snyder, Amanda M ; Wang, XinSheng ; Patton, Stephanie M ; Arosio, Paolo ; Levi, Sonia ; Earley, Christopher J ; Allen, Richard P ; Connor, James R

Journal of neuropathology and experimental neurology, 2009-11, Vol.68 (11), p.1193-1199 [Periódico revisado por pares]

Hagerstown, MD: American Association of Neuropathologists, Inc

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9
TBX22 mutations are a frequent cause of cleft palate
TBX22 mutations are a frequent cause of cleft palate
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TBX22 mutations are a frequent cause of cleft palate

Marçano, A C B ; Doudney, K ; Braybrook, C ; Squires, R ; Patton, M A ; Lees, M M ; Richieri-Costa, A ; Lidral, A C ; Murray, J C ; Moore, G E ; Stanier, P

Journal of medical genetics, 2004-01, Vol.41 (1), p.68-74 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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10
Decreased transferrin receptor expression by neuromelanin cells in restless legs syndrome
Decreased transferrin receptor expression by neuromelanin cells in restless legs syndrome
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Decreased transferrin receptor expression by neuromelanin cells in restless legs syndrome

CONNOR, J. R ; WANG, X. S ; PATTON, S. M ; MENZIES, S. L ; TRONCOSO, J. C ; EARLEY, C. J ; ALLEN, R. P

Neurology, 2004-05, Vol.62 (9), p.1563-1567 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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