skip to main content

Results 1 - 10 of 53  for Great Falls College MSU

Results 1 2 3 4 5 next page
Show only
Refined by: topic: Nervous System Diseases remove topic: Mutation remove
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Material Type:
Article
Add to e-Shelf

Spinocerebellar Ataxia-21 in a Turkish Child

Incecik, Faruk ; Herguner, Ozlem M ; Willems, Patrick ; Mungan, Neslihan O

Annals of Indian Academy of Neurology, 2018, Vol.21(1), p.68-70 [Peer Reviewed Journal]

Full text available

View all versions
2
Material Type:
Article
Add to e-Shelf

Use of Acetazolamide in Sulfonamide-Allergic Patients With Neurologic Channelopathies

Platt, Daniel ; Griggs, Robert Platt, Daniel (correspondence author)

Archives of Neurology, 2012, Vol.69(4), pp.527-529 [Peer Reviewed Journal]

No full-text

View all versions
3
Material Type:
Article
Add to e-Shelf

Primary diagnosis of Wolfram syndrome in an adult patient - Case report and description of a novel pathogenic mutation

Waschbisch, Anne ; Volbers, Bastian ; Struffert, Tobias ; Hoyer, Juliane ; Schwab, Stefan ; Bardutzky, Juergen Waschbisch, Anne (correspondence author)

Journal of the Neurological Sciences, Jan 15, 2011, Vol.300(1-2), pp.191-193 [Peer Reviewed Journal]

No full-text

View all versions
4
Material Type:
Article
Add to e-Shelf

Novel Mitochondrial C15620A Variant may Modulate the Phenotype of Mitochondrial G11778A Mutation in a Chinese Family with Leigh Syndrome

Ji, Kunqian ; Zheng, Jinfan ; Sun, Baoying ; Liu, Fuchen ; Shan, Jingli ; Li, Duoling ; Luo, Yue-Bei ; Zhao, Yuying ; Yan, Chuanzhu Ji, Kunqian (correspondence author)

Neuromolecular Medicine, Mar 2014, Vol.16(1), pp.119-126 [Peer Reviewed Journal]

Full text available

View all versions
5
Material Type:
Article
Add to e-Shelf

Severe congenital neutropenia with neurological impairment due to a homozygous VPS45 p.E238K mutation: A case report suggesting a genotype-phenotype correlation

Meerschaut, Ilse ; Bordon, Victoria ; Dhooge, Catharina ; Delbeke, Patricia ; Vanlander, Arnaud ; Simon, Amos ; Klein, Christoph ; Kooy, Rfrank ; Somech, Raz ; Callewaert, Bert Meerschaut, Ilse (correspondence author)

American Journal of Medical Genetics Part A, December 2015, Vol.167(12), pp.3214-3218 [Peer Reviewed Journal]

Full text available

View all versions
6
Material Type:
Article
Add to e-Shelf

Coexistence of a T118M PMP22 missense mutation and chromosome 17 (17p11.2-p12) deletion

Jerath, Nivedita ; Kamholz, John ; Grider, Tiffany ; Harper, Amy ; Swenson, Andrea ; Shy, Michael Jerath, Nivedita (correspondence author)

Muscle & Nerve, November 2015, Vol.52(5), pp.905-908 [Peer Reviewed Journal]

Full text available

View all versions
7
Material Type:
Article
Add to e-Shelf

Adrenocortical carcinoma and succinate dehydrogenase gene mutations: an observational case series

Else, Tobias ; Lerario, Antonio ; Everett, Jessica ; Haymon, Lori ; Wham, Deborah ; Mullane, Michael ; Wilson, Tremika ; Rainville, Irene ; Rana, Huma ; Worth, Andrew ; Snyder, Nathaniel ; Blair, Ian ; Mckay, Rana ; Kilbridge, Kerry ; Hammer, Gary ; Barletta, Justine ; Vaidya, Anand

European Journal of Endocrinology, Nov 2017, Vol.177(5), p.439 [Peer Reviewed Journal]

Full text available

View all versions
8
Material Type:
Article
Add to e-Shelf

The Association of Pseudohypoparathyroidism Type Ia with Chiari Malformation Type I: A Coincidence or a Common Link?

Kashani, Paria ; Roy, Madan ; Gillis, Linda ; Ajani, Olufemi ; Samaan, M. Constantine

Case Reports in Medicine, 2016, Vol.2016 [Peer Reviewed Journal]

Full text available

View all versions
9
Material Type:
Article
Add to e-Shelf

Neurologic Adverse Effects of Ranolazine in an Elderly Patient with Renal Impairment

Southard, Robert ; M Blum, Rachel ; Bui, An ; Blankstein, Ron Southard, Robert (correspondence author)

Pharmacotherapy, Jan 2013, Vol.33(1), pp.e9-e13 [Peer Reviewed Journal]

Full text available

View all versions
10
Material Type:
Article
Add to e-Shelf

A case of neuromyotonia and axonal motor neuropathy: A report of a HINT1 mutation in the United States

Jerath, Nivedita ; Shy, Michael ; Grider, Tiffany ; Gutmann, Ludwig Jerath, Nivedita (correspondence author)

Muscle & Nerve, December 2015, Vol.52(6), pp.1110-1113 [Peer Reviewed Journal]

Full text available

View all versions

Results 1 - 10 of 53  for Great Falls College MSU

Results 1 2 3 4 5 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Show only

  1. Full Text Online (42)

Refine My Results

Topic 

  1. Humans  (31)
  2. Medicine  (30)
  3. Case Report  (29)
  4. Case Reports  (29)
  5. Female  (26)
  6. Male  (18)
  7. Patients  (15)
  8. Adult  (14)
  9. Nuclear Magnetic Resonance  (13)
  10. Age  (13)
  11. Magnetic Resonance Imaging  (12)
  12. Ataxia  (12)
  13. Brain  (11)
  14. Gene Mutation  (10)
  15. Child  (9)
  16. Mutation–Genetics  (9)
  17. Neurology  (8)
  18. Epilepsy  (8)
  19. Neurogenetics  (6)
  20. More options open sub menu

Creation Date 

From To
  1. Before 2006  (4)
  2. 2006 To 2010  (5)
  3. 2011 To 2013  (6)
  4. 2014 To 2017  (24)
  5. After 2017  (14)
  6. More options open sub menu

Suggested New Searches

Ignore my query and look for everything

by this author/creator:

  1. Incecik, Faruk
  2. Dastsooz, Hassan
  3. O'Brien, D.P.
  4. Grider, Tiffany
  5. Nemati, Hamid

Searching Remote Databases, Please Wait