Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 128 entries
Sorted by: Best Match Show Resources per page
The natural history of COPD: confirming and going beyond Fletcher and Peto.

The European respiratory journal

Miller A, Raskin JM.
PMID: 25082904
Eur Respir J. 2014 Aug;44(2):280-3. doi: 10.1183/09031936.00079514.

No abstract available.

Cite
Miller A, Raskin JM. The natural history of COPD: confirming and going beyond Fletcher and Peto. Eur Respir J. 2014;44(2):280-3doi: 10.1183/09031936.00079514.
Miller, A., & Raskin, J. M. (2014). The natural history of COPD: confirming and going beyond Fletcher and Peto. The European respiratory journal, 44(2), 280-3. https://doi.org/10.1183/09031936.00079514
Miller, Albert, and Raskin, Jonathan M. "The natural history of COPD: confirming and going beyond Fletcher and Peto." The European respiratory journal vol. 44,2 (2014): 280-3. doi: https://doi.org/10.1183/09031936.00079514
Miller A, Raskin JM. The natural history of COPD: confirming and going beyond Fletcher and Peto. Eur Respir J. 2014 Aug;44(2):280-3. doi: 10.1183/09031936.00079514. PMID: 25082904.
Copy Download .nbib Format: NLM
Review topics.

Orthopedics

Raskin SP.
PMID: 24822741
Orthopedics. 1980 Oct 01;3(10):1011-23. doi: 10.3928/0147-7447-19801001-11.

No abstract available.

Cite
Raskin SP. Review topics. Orthopedics. 1980;3(10):1011-23doi: 10.3928/0147-7447-19801001-11.
Raskin, S. P. (1980). Review topics. Orthopedics, 3(10), 1011-23. https://doi.org/10.3928/0147-7447-19801001-11
Raskin, S P. "Review topics." Orthopedics vol. 3,10 (1980): 1011-23. doi: https://doi.org/10.3928/0147-7447-19801001-11
Raskin SP. Review topics. Orthopedics. 1980 Oct 01;3(10):1011-23. doi: 10.3928/0147-7447-19801001-11. PMID: 24822741.
Copy Download .nbib Format: NLM
The Effects of Stress Exposure on Prefrontal Cortex: Translating Basic Research into Successful Treatments for Post-Traumatic Stress Disorder.

Neurobiology of stress

Arnsten AF, Raskind MA, Taylor FB, Connor DF.
PMID: 25436222
Neurobiol Stress. 2015 Jan 01;1:89-99. doi: 10.1016/j.ynstr.2014.10.002.

Research on the neurobiology of the stress response in animals has led to successful new treatments for Post-Traumatic Stress Disorder (PTSD) in humans. Basic research has found that high levels of catecholamine release during stress rapidly impair the top-down...

Cite
Arnsten AF, Raskind MA, Taylor FB, et al. The Effects of Stress Exposure on Prefrontal Cortex: Translating Basic Research into Successful Treatments for Post-Traumatic Stress Disorder. Neurobiol Stress. 2015;1:89-99doi: 10.1016/j.ynstr.2014.10.002.
Arnsten, A. F., Raskind, M. A., Taylor, F. B., & Connor, D. F. (2015). The Effects of Stress Exposure on Prefrontal Cortex: Translating Basic Research into Successful Treatments for Post-Traumatic Stress Disorder. Neurobiology of stress, 189-99. https://doi.org/10.1016/j.ynstr.2014.10.002
Arnsten, Amy F T, et al. "The Effects of Stress Exposure on Prefrontal Cortex: Translating Basic Research into Successful Treatments for Post-Traumatic Stress Disorder." Neurobiology of stress vol. 1 (2015): 89-99. doi: https://doi.org/10.1016/j.ynstr.2014.10.002
Arnsten AF, Raskind MA, Taylor FB, Connor DF. The Effects of Stress Exposure on Prefrontal Cortex: Translating Basic Research into Successful Treatments for Post-Traumatic Stress Disorder. Neurobiol Stress. 2015 Jan 01;1:89-99. doi: 10.1016/j.ynstr.2014.10.002. PMID: 25436222; PMCID: PMC4244027.
Copy Download .nbib Format: NLM
Segregation analysis of phenotypic components of learning disabilities. II. Phonological decoding.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

Chapman NH, Raskind WH, Thomson JB, Berninger VW, Wijsman EM.
PMID: 12898577
Am J Med Genet B Neuropsychiatr Genet. 2003 Aug 15;121(1):60-70. doi: 10.1002/ajmg.b.20068.

Dyslexia is a common, complex disorder, which is thought to have a genetic component. The study of the genetics of dyslexia is complicated by a lack of consensus on diagnostic criteria, and the probability of genetic heterogeneity-it is possible...

Cite
Chapman NH, Raskind WH, Thomson JB, et al. Segregation analysis of phenotypic components of learning disabilities. II. Phonological decoding. Am J Med Genet B Neuropsychiatr Genet. 2003;121(1):60-70doi: 10.1002/ajmg.b.20068.
Chapman, N. H., Raskind, W. H., Thomson, J. B., Berninger, V. W., & Wijsman, E. M. (2003). Segregation analysis of phenotypic components of learning disabilities. II. Phonological decoding. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 121(1), 60-70. https://doi.org/10.1002/ajmg.b.20068
Chapman, Nicola H, et al. "Segregation analysis of phenotypic components of learning disabilities. II. Phonological decoding." American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 121,1 (2003): 60-70. doi: https://doi.org/10.1002/ajmg.b.20068
Chapman NH, Raskind WH, Thomson JB, Berninger VW, Wijsman EM. Segregation analysis of phenotypic components of learning disabilities. II. Phonological decoding. Am J Med Genet B Neuropsychiatr Genet. 2003 Aug 15;121(1):60-70. doi: 10.1002/ajmg.b.20068. PMID: 12898577.
Copy Download .nbib Format: NLM
Spin-on spintronics: ultrafast electron spin dynamics in ZnO and Zn₁-xCoxO sol-gel films.

Nano letters

Whitaker KM, Raskin M, Kiliani G, Beha K, Ochsenbein ST, Janssen N, Fonin M, Rüdiger U, Leitenstorfer A, Gamelin DR, Bratschitsch R.
PMID: 21749121
Nano Lett. 2011 Aug 10;11(8):3355-60. doi: 10.1021/nl201736p. Epub 2011 Jul 19.

We use time-resolved Faraday rotation spectroscopy to probe the electron spin dynamics in ZnO and magnetically doped Zn(1-x)Co(x)O sol-gel thin films. In undoped ZnO, we observe an anomalous temperature dependence of the ensemble spin dephasing time T(2), i.e., longer...

Cite
Whitaker KM, Raskin M, Kiliani G, et al. Spin-on spintronics: ultrafast electron spin dynamics in ZnO and Zn₁-xCoxO sol-gel films. Nano Lett. 2011;11(8):3355-60doi: 10.1021/nl201736p.
Whitaker, K. M., Raskin, M., Kiliani, G., Beha, K., Ochsenbein, S. T., Janssen, N., Fonin, M., Rüdiger, U., Leitenstorfer, A., Gamelin, D. R., & Bratschitsch, R. (2011). Spin-on spintronics: ultrafast electron spin dynamics in ZnO and Zn₁-xCoxO sol-gel films. Nano letters, 11(8), 3355-60. https://doi.org/10.1021/nl201736p
Whitaker, Kelly M, et al. "Spin-on spintronics: ultrafast electron spin dynamics in ZnO and Zn₁-xCoxO sol-gel films." Nano letters vol. 11,8 (2011): 3355-60. doi: https://doi.org/10.1021/nl201736p
Whitaker KM, Raskin M, Kiliani G, Beha K, Ochsenbein ST, Janssen N, Fonin M, Rüdiger U, Leitenstorfer A, Gamelin DR, Bratschitsch R. Spin-on spintronics: ultrafast electron spin dynamics in ZnO and Zn₁-xCoxO sol-gel films. Nano Lett. 2011 Aug 10;11(8):3355-60. doi: 10.1021/nl201736p. Epub 2011 Jul 19. PMID: 21749121.
Copy Download .nbib Format: NLM
Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.

Journal of neurodevelopmental disorders

Peter B, Raskind WH, Matsushita M, Lisowski M, Vu T, Berninger VW, Wijsman EM, Brkanac Z.
PMID: 21484596
J Neurodev Disord. 2011 Mar;3(1):39-49. doi: 10.1007/s11689-010-9065-0. Epub 2010 Nov 09.

Two functionally related genes, FOXP2 and CNTNAP2, influence language abilities in families with rare syndromic and common nonsyndromic forms of impaired language, respectively. We investigated whether these genes are associated with component phenotypes of dyslexia and measures of sequential...

Cite
Peter B, Raskind WH, Matsushita M, et al. Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample. J Neurodev Disord. 2010;3(1):39-49doi: 10.1007/s11689-010-9065-0.
Peter, B., Raskind, W. H., Matsushita, M., Lisowski, M., Vu, T., Berninger, V. W., Wijsman, E. M., & Brkanac, Z. (2011). Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample. Journal of neurodevelopmental disorders, 3(1), 39-49. https://doi.org/10.1007/s11689-010-9065-0
Peter, Beate, et al. "Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample." Journal of neurodevelopmental disorders vol. 3,1 (2011): 39-49. doi: https://doi.org/10.1007/s11689-010-9065-0
Peter B, Raskind WH, Matsushita M, Lisowski M, Vu T, Berninger VW, Wijsman EM, Brkanac Z. Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample. J Neurodev Disord. 2011 Mar;3(1):39-49. doi: 10.1007/s11689-010-9065-0. Epub 2010 Nov 09. PMID: 21484596; PMCID: PMC3163991.
Copy Download .nbib Format: NLM
Na(2/7)Gd(4/7)MoO4: a modulated scheelite-type structure and conductivity properties.

Inorganic chemistry

Morozov V, Arakcheeva A, Redkin B, Sinitsyn V, Khasanov S, Kudrenko E, Raskina M, Lebedev O, Van Tendeloo G.
PMID: 22515515
Inorg Chem. 2012 May 07;51(9):5313-24. doi: 10.1021/ic300221m. Epub 2012 Apr 19.

Scheelite-type compounds with the general formula (A1,A2)(n)[(B1,B2)O(4)](m) (2/3 ≤ n/m ≤ 3/2) are the subject of large interest owing to their stability, relatively simple preparation, and optical properties. The creation of cation vacancies (□) in the scheelite-type framework and...

Cite
Morozov V, Arakcheeva A, Redkin B, et al. Na(2/7)Gd(4/7)MoO4: a modulated scheelite-type structure and conductivity properties. Inorg Chem. 2012;51(9):5313-24doi: 10.1021/ic300221m.
Morozov, V., Arakcheeva, A., Redkin, B., Sinitsyn, V., Khasanov, S., Kudrenko, E., Raskina, M., Lebedev, O., & Van Tendeloo, G. (2012). Na(2/7)Gd(4/7)MoO4: a modulated scheelite-type structure and conductivity properties. Inorganic chemistry, 51(9), 5313-24. https://doi.org/10.1021/ic300221m
Morozov, V, et al. "Na(2/7)Gd(4/7)MoO4: a modulated scheelite-type structure and conductivity properties." Inorganic chemistry vol. 51,9 (2012): 5313-24. doi: https://doi.org/10.1021/ic300221m
Morozov V, Arakcheeva A, Redkin B, Sinitsyn V, Khasanov S, Kudrenko E, Raskina M, Lebedev O, Van Tendeloo G. Na(2/7)Gd(4/7)MoO4: a modulated scheelite-type structure and conductivity properties. Inorg Chem. 2012 May 07;51(9):5313-24. doi: 10.1021/ic300221m. Epub 2012 Apr 19. PMID: 22515515.
Copy Download .nbib Format: NLM
Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular characterization of a new contiguous gene syndrome.

Genetics and molecular biology

Souza J, Faucz F, Sotomaior V, Filho AB, Rosenfeld J, Raskin S.
PMID: 22215957
Genet Mol Biol. 2011 Oct;34(4):557-61. doi: 10.1590/S1415-47572011005000044. Epub 2011 Oct 01.

The Peutz-Jeghers syndrome (PJS) is an autosomal-dominant hamartomatous polyposis syndrome characterized by mucocutaneous pigmentation, gastrointestinal polyps and the increased risk of multiple cancers. The causative point mutation in the STK11 gene of most patients accounts for about 30% of...

Cite
Souza J, Faucz F, Sotomaior V, et al. Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular characterization of a new contiguous gene syndrome. Genet Mol Biol. 2011;34(4):557-61doi: 10.1590/S1415-47572011005000044.
Souza, J., Faucz, F., Sotomaior, V., Filho, A. B., Rosenfeld, J., & Raskin, S. (2011). Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular characterization of a new contiguous gene syndrome. Genetics and molecular biology, 34(4), 557-61. https://doi.org/10.1590/S1415-47572011005000044
Souza, Josiane, et al. "Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular characterization of a new contiguous gene syndrome." Genetics and molecular biology vol. 34,4 (2011): 557-61. doi: https://doi.org/10.1590/S1415-47572011005000044
Souza J, Faucz F, Sotomaior V, Filho AB, Rosenfeld J, Raskin S. Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular characterization of a new contiguous gene syndrome. Genet Mol Biol. 2011 Oct;34(4):557-61. doi: 10.1590/S1415-47572011005000044. Epub 2011 Oct 01. PMID: 22215957; PMCID: PMC3229108.
Copy Download .nbib Format: NLM
Sequential Loss of LC Noradrenergic and Dopaminergic Neurons Results in a Correlation of Dopaminergic Neuronal Number to Striatal Dopamine Concentration.

Frontiers in pharmacology

Szot P, Franklin A, Sikkema C, Wilkinson CW, Raskind MA.
PMID: 23129999
Front Pharmacol. 2012 Oct 22;3:184. doi: 10.3389/fphar.2012.00184. eCollection 2012.

Noradrenergic neurons in the locus coeruleus (LC) are significantly reduced in Parkinson's disease (PD) and the LC exhibits neuropathological changes early in the disease process. It has been suggested that a loss of LC neurons can enhance the susceptibility...

Cite
Szot P, Franklin A, Sikkema C, et al. Sequential Loss of LC Noradrenergic and Dopaminergic Neurons Results in a Correlation of Dopaminergic Neuronal Number to Striatal Dopamine Concentration. Front Pharmacol. 2012;3:184doi: 10.3389/fphar.2012.00184.
Szot, P., Franklin, A., Sikkema, C., Wilkinson, C. W., & Raskind, M. A. (2012). Sequential Loss of LC Noradrenergic and Dopaminergic Neurons Results in a Correlation of Dopaminergic Neuronal Number to Striatal Dopamine Concentration. Frontiers in pharmacology, 3184. https://doi.org/10.3389/fphar.2012.00184
Szot, Patricia, et al. "Sequential Loss of LC Noradrenergic and Dopaminergic Neurons Results in a Correlation of Dopaminergic Neuronal Number to Striatal Dopamine Concentration." Frontiers in pharmacology vol. 3 (2012): 184. doi: https://doi.org/10.3389/fphar.2012.00184
Szot P, Franklin A, Sikkema C, Wilkinson CW, Raskind MA. Sequential Loss of LC Noradrenergic and Dopaminergic Neurons Results in a Correlation of Dopaminergic Neuronal Number to Striatal Dopamine Concentration. Front Pharmacol. 2012 Oct 22;3:184. doi: 10.3389/fphar.2012.00184. eCollection 2012. PMID: 23129999; PMCID: PMC3487487.
Copy Download .nbib Format: NLM
Kohlschütter-Tönz syndrome in siblings without ROGDI mutation.

Oral health and dental management

De Souza CM, Souza J, Furtado CM, Cleto JL, Antoniuk SA, Raskin S.
PMID: 25284547
Oral Health Dent Manag. 2014 Sep;13(3):728-30.

BACKGROUND: Kohlschütter-Tönz syndrome is a rare neurodegenerative disorder presenting with intractable seizures, developmental regression, and characteristic hypoplastic dental enamel indicative of amelogenesis imperfecta. Recently, mutations in ROGDI were identified in part of Kohlschütter-Tönz syndrome cases, but the siblings reported...

Cite
De Souza CM, Souza J, Furtado CM, et al. Kohlschütter-Tönz syndrome in siblings without ROGDI mutation. Oral Health Dent Manag. 2014;13(3):728-30
De Souza, C. M., Souza, J., Furtado, C. M., Cleto, J. L., Antoniuk, S. A., & Raskin, S. (2014). Kohlschütter-Tönz syndrome in siblings without ROGDI mutation. Oral health and dental management, 13(3), 728-30.
De Souza, C M, et al. "Kohlschütter-Tönz syndrome in siblings without ROGDI mutation." Oral health and dental management vol. 13,3 (2014): 728-30.
De Souza CM, Souza J, Furtado CM, Cleto JL, Antoniuk SA, Raskin S. Kohlschütter-Tönz syndrome in siblings without ROGDI mutation. Oral Health Dent Manag. 2014 Sep;13(3):728-30. PMID: 25284547.
Copy Download .nbib Format: NLM
Verrucous Hemangioma of the Plantar Surface of the Foot: A Case Report.

JBJS case connector

Haskins SM, Shields NN.
PMID: 29252556
JBJS Case Connect. 2014 Jan 22;4(1):e10. doi: 10.2106/JBJS.CC.M.00132.

No abstract available.

Cite
Haskins SM, Shields NN. Verrucous Hemangioma of the Plantar Surface of the Foot: A Case Report. JBJS Case Connect. 2014;4(1):e10doi: 10.2106/JBJS.CC.M.00132.
Haskins, S. M., & Shields, N. N. (2014). Verrucous Hemangioma of the Plantar Surface of the Foot: A Case Report. JBJS case connector, 4(1), e10. https://doi.org/10.2106/JBJS.CC.M.00132
Haskins, Scott M, and Shields, Naomi N. "Verrucous Hemangioma of the Plantar Surface of the Foot: A Case Report." JBJS case connector vol. 4,1 (2014): e10. doi: https://doi.org/10.2106/JBJS.CC.M.00132
Haskins SM, Shields NN. Verrucous Hemangioma of the Plantar Surface of the Foot: A Case Report. JBJS Case Connect. 2014 Jan 22;4(1):e10. doi: 10.2106/JBJS.CC.M.00132. PMID: 29252556.
Copy Download .nbib Format: NLM
Heavy Drinking in College Students Is Associated with Accelerated Gray Matter Volumetric Decline over a 2 Year Period.

Frontiers in behavioral neuroscience

Meda SA, Dager AD, Hawkins KA, Tennen H, Raskin S, Wood RM, Austad CS, Fallahi CR, Pearlson GD.
PMID: 29033801
Front Behav Neurosci. 2017 Sep 29;11:176. doi: 10.3389/fnbeh.2017.00176. eCollection 2017.

No abstract available.

Cite
Meda SA, Dager AD, Hawkins KA, et al. Heavy Drinking in College Students Is Associated with Accelerated Gray Matter Volumetric Decline over a 2 Year Period. Front Behav Neurosci. 2017;11:176doi: 10.3389/fnbeh.2017.00176.
Meda, S. A., Dager, A. D., Hawkins, K. A., Tennen, H., Raskin, S., Wood, R. M., Austad, C. S., Fallahi, C. R., & Pearlson, G. D. (2017). Heavy Drinking in College Students Is Associated with Accelerated Gray Matter Volumetric Decline over a 2 Year Period. Frontiers in behavioral neuroscience, 11176. https://doi.org/10.3389/fnbeh.2017.00176
Meda, Shashwath A, et al. "Heavy Drinking in College Students Is Associated with Accelerated Gray Matter Volumetric Decline over a 2 Year Period." Frontiers in behavioral neuroscience vol. 11 (2017): 176. doi: https://doi.org/10.3389/fnbeh.2017.00176
Meda SA, Dager AD, Hawkins KA, Tennen H, Raskin S, Wood RM, Austad CS, Fallahi CR, Pearlson GD. Heavy Drinking in College Students Is Associated with Accelerated Gray Matter Volumetric Decline over a 2 Year Period. Front Behav Neurosci. 2017 Sep 29;11:176. doi: 10.3389/fnbeh.2017.00176. eCollection 2017. PMID: 29033801; PMCID: PMC5627037.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 128 entries