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Deep Brain Stimulation for Pediatric Dystonia: A Review of the Literature and Suggested Programming Algorithm.
Published in:
Journal of Child Neurology, 2022, v. 37, n. 10/11, p. 813, doi. 10.1177/08830738221115248
By:
- Gelineau-Morel, Rose;
- Kruer, Michael C.;
- Garris, Jordan F.;
- Abu Libdeh, Amal;
- Barbosa, Daniel A. N.;
- Coffman, Keith A.;
- Moon, David;
- Barton, Christopher;
- Zea Vera, Alonso;
- Bruce, Adrienne B.;
- Larsh, Travis;
- Wu, Steve W.;
- Gilbert, Donald L.;
- O'Malley, Jennifer A.
Publication type:
Article
Brown-Vialetto-Van Laere Syndrome as a Mimic of Neuroimmune Disorders: 3 Cases From the Clinic and Review of the Literature.
Published in:
Journal of Child Neurology, 2017, v. 32, n. 6, p. 528, doi. 10.1177/0883073816689517
By:
- Allison, Tyler;
- Roncero, Inés;
- Forsyth, Rob;
- Coffman, Keith;
- Pichon, Jean-Baptiste Le
Publication type:
Article
Pial Synangiosis Ameliorates Movement Disorders in the Absence of Prior Stroke in Moyamoya Disease.
Published in:
Journal of Child Neurology, 2016, v. 31, n. 5, p. 646, doi. 10.1177/0883073815609152
By:
- Greene, Stephanie;
- Bansal, Lalit;
- Coffman, Keith A.;
- Nardone, Raffaele;
- Zuccoli, Giulio
Publication type:
Article
Variants in the zinc transporter TMEM163 cause a hypomyelinating leukodystrophy.
Published in:
Brain: A Journal of Neurology, 2022, v. 145, n. 12, p. 4202, doi. 10.1093/brain/awac295
By:
- Rosario, Michelle C do;
- Bey, Guillermo Rodriguez;
- Nmezi, Bruce;
- Liu, Fang;
- Oranburg, Talia;
- Cohen, Ana S A;
- Coffman, Keith A;
- Brown, Maya R;
- Kiselyov, Kirill;
- Waisfisz, Quinten;
- Flohil, Myrthe T;
- Siddiqui, Shahyan;
- Rosenfeld, Jill A;
- Iglesias, Alejandro;
- Girisha, Katta Mohan;
- Wolf, Nicole I;
- Padiath, Quasar Saleem;
- Shukla, Anju
Publication type:
Article
Deletion of conserved non‐coding sequences downstream from NKX2‐1: A novel disease‐causing mechanism for benign hereditary chorea.
Published in:
Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 4, p. 1, doi. 10.1002/mgg3.1647
By:
- Liao, Jun;
- Coffman, Keith A.;
- Locker, Joseph;
- Padiath, Quasar S.;
- Nmezi, Bruce;
- Filipink, Robyn A.;
- Hu, Jie;
- Sathanoori, Malini;
- Madan‐Khetarpal, Suneeta;
- McGuire, Marianne;
- Schreiber, Allison;
- Moran, Rocio;
- Friedman, Neil;
- Hoffner, Lori;
- Rajkovic, Aleksandar;
- Yatsenko, Svetlana A.;
- Surti, Urvashi
Publication type:
Article
Diagnosis and Management of Functional Tic-Like Phenomena.
Published in:
Journal of Clinical Medicine, 2022, v. 11, n. 21, p. 6470, doi. 10.3390/jcm11216470
By:
- Malaty, Irene A.;
- Anderson, Seonaid;
- Bennett, Shannon M.;
- Budman, Cathy L.;
- Coffey, Barbara J.;
- Coffman, Keith A.;
- Greenberg, Erica;
- McGuire, Joseph F.;
- Müller-Vahl, Kirsten R.;
- Okun, Michael S.;
- Quezada, Julio;
- Robichaux-Viehoever, Amy;
- Black, Kevin J.
Publication type:
Article
Current Approaches and New Developments in the Pharmacological Management of Tourette Syndrome.
Published in:
2018
By:
- Quezada, Julio;
- Coffman, Keith A.
Publication type:
journal article
Dysautonomia and functional impairment in rare developmental and epileptic encephalopathies: the other nervous system.
Published in:
Developmental Medicine & Child Neurology, 2021, v. 63, n. 12, p. 1433, doi. 10.1111/dmcn.14990
By:
- Berg, Anne T;
- Coffman, Keith;
- Gaebler‐Spira, Deborah
Publication type:
Article
Heterocycle-to-Heterocycle Route to Quinoline-4-amines: Reductive Heterocyclization of 3-(2-Nitrophenyl)isoxazoles.
Published in:
European Journal of Organic Chemistry, 2014, v. 2014, n. 34, p. 7651, doi. 10.1002/ejoc.201403065
By:
- Coffman, Keith C.;
- Duong, Vy;
- Bagdasarian, Alex L.;
- Fettinger, James C.;
- Haddadin, Makhluf J.;
- Kurth, Mark J.
Publication type:
Article
Loss of Function Variants in Human PNPLA8 Encoding Calcium-Independent Phospholipase A2γ Recapitulate the Mitochondriopathy of the Homologous Null Mouse.
Published in:
Human Mutation, 2015, v. 36, n. 6, p. 656, doi. 10.1002/humu.22790
By:
- Saunders, Carol J.;
- Moon, Sung Ho;
- Liu, Xinping;
- Thiffault, Isabelle;
- Coffman, Keith;
- LePichon, Jean‐Baptiste;
- Taboada, Eugenio;
- Smith, Laurie D.;
- Farrow, Emily G.;
- Miller, Neil;
- Gibson, Margaret;
- Patterson, Melanie;
- Kingsmore, Stephen F.;
- Gross, Richard W.
Publication type:
Article
Loss of Function Variants in Human PNPLA8 Encoding Calcium-Independent Phospholipase A2γ Recapitulate the Mitochondriopathy of the Homologous Null Mouse.
Published in:
Human Mutation, 2015, v. 36, n. 3, p. 301, doi. 10.1002/humu.22743
By:
- Saunders, Carol J.;
- Moon, Sung Ho;
- Liu, Xinping;
- Thiffault, Isabelle;
- Coffman, Keith;
- LePichon, Jean‐Baptiste;
- Taboada, Eugenio;
- Smith, Laurie D.;
- Farrow, Emily G.;
- Miller, Neil;
- Gibson, Margaret;
- Patterson, Melanie;
- Kingsmore, Stephen F.;
- Gross, Richard W.
Publication type:
Article
Moving the Plasmon of LaB6 from IR to Near-IR via Eu-Doping.
Published in:
Materials (1996-1944), 2018, v. 11, n. 2, p. 226, doi. 10.3390/ma11020226
By:
- Mattox, Tracy M.;
- Coffman, D. Keith;
- Roh, Inwhan;
- Sims, Christopher;
- Urban, Jeffrey J.
Publication type:
Article
Orthogonally Protected Thiazole and Isoxazole Diamino Acids: An Efficient Synthetic Route.
Published in:
Chemistry - A European Journal, 2010, v. 16, n. 30, p. 9002, doi. 10.1002/chem.201001492
By:
- Butler, Jeffrey D.;
- Coffman, Keith C.;
- Ziebart, Kristin T.;
- Toney, Michael D.;
- Kurth, Mark J.
Publication type:
Article
Ecopipam, a D1 receptor antagonist, for treatment of tourette syndrome in children: A randomized, placebo-controlled crossover study.
Published in:
2018
By:
- Gilbert, Donald L.;
- Murphy, Tanya K.;
- Jankovic, Joseph;
- Budman, Cathy L.;
- Black, Kevin J.;
- Kurlan, Roger M.;
- Coffman, Keith A.;
- McCracken, James T.;
- Juncos, Jorge;
- Grant, Jon E.;
- Chipkin, Richard E.
Publication type:
journal article

Found: 14

Deep Brain Stimulation for Pediatric Dystonia: A Review of the Literature and Suggested Programming Algorithm.

Brown-Vialetto-Van Laere Syndrome as a Mimic of Neuroimmune Disorders: 3 Cases From the Clinic and Review of the Literature.

Pial Synangiosis Ameliorates Movement Disorders in the Absence of Prior Stroke in Moyamoya Disease.

Variants in the zinc transporter TMEM163 cause a hypomyelinating leukodystrophy.

Deletion of conserved non‐coding sequences downstream from NKX2‐1: A novel disease‐causing mechanism for benign hereditary chorea.

Diagnosis and Management of Functional Tic-Like Phenomena.

Current Approaches and New Developments in the Pharmacological Management of Tourette Syndrome.

Dysautonomia and functional impairment in rare developmental and epileptic encephalopathies: the other nervous system.

Heterocycle-to-Heterocycle Route to Quinoline-4-amines: Reductive Heterocyclization of 3-(2-Nitrophenyl)isoxazoles.

Loss of Function Variants in Human PNPLA8 Encoding Calcium-Independent Phospholipase A<sub>2</sub>γ Recapitulate the Mitochondriopathy of the Homologous Null Mouse.

Loss of Function Variants in Human PNPLA8 Encoding Calcium-Independent Phospholipase A<sub>2</sub>γ Recapitulate the Mitochondriopathy of the Homologous Null Mouse.

Moving the Plasmon of LaB<sub>6</sub> from IR to Near-IR via Eu-Doping.

Orthogonally Protected Thiazole and Isoxazole Diamino Acids: An Efficient Synthetic Route.

Ecopipam, a D1 receptor antagonist, for treatment of tourette syndrome in children: A randomized, placebo-controlled crossover study.