Results 71 to 80 of about 1,346,685 (174)

Phenotypic Clues in Infantile‐Onset Parkinsonism‐Dystonia‐2: A Treatable Neurotransmitter Disorder

Movement Disorders Clinical Practice, Volume 13, Issue 9, Page 2288-2292, September 2026.
Sangeetha Yoganathan, Haya S. AlFaris, Lindsey Vogt, Michele Eid, Anika Menetrey, Sayoni Roy Chowdhury, Dawn Codeiro, Pradeep Krishnan, Liali Aljouda, Emily W.Y. Tam, Carolina Gorodetsky   +10 more
wiley   +1 more source

Aripiprazole-induced oculogyric crisis (acute dystonia) in 11 years old girl: a case report

, 2020
noneAbstract Acute dystonic reaction which is described as involuntary muscle spasms and contractions including neck, chin, eye and mouth muscles is an extrapyramidal adverse effect.
Çiçek, Ayla Uzun, Sarı, Seda Aybüke, Işık, Cansu Mercan, Demirci, Belde   +3 more
core   +1 more source

A Japanese Pregnant Woman With Treatment‐Resistant Schizophrenia Who Continued Clozapine With Blood Concentration Monitoring During the Perinatal Period and Had a Healthy Baby: A Case Report

Neuropsychopharmacology Reports, Volume 45, Issue 4, December 2025.
This is the first case in Japan where a patient with treatment‐resistant schizophrenia planned marriage and pregnancy while on clozapine treatment, continued clozapine with blood level monitoring throughout the perinatal period and had a healthy baby.
Mariko Tsukiji, Kaori Yamazaki, Yusuke Nakata, Tsuyoshi Sasaki, Keita Idemoto, Kazuki Okada, Shingo Yamazaki, Akiko Omoto, Kaori Koga, Tomihisa Niitsu, Itsuko Ishii   +10 more
wiley   +1 more source

WWOX Mutation as a Rare Cause of Neonatal‐Infantile Parkinsonism Mimicking a Neurotransmitter Disorder: A Case Report

Journal of Paediatrics and Child Health, Volume 62, Issue 7, Page 1273-1277, July 2026.
Ozge Serce Pehlevan, Gizem Gider Yaman, Anıl Gok, Leman Tekin Orgun   +3 more
wiley   +1 more source

Consensus Guideline for the Diagnosis and Treatment of Tyrosine Hydroxylase (TH) Deficiency

Journal of Inherited Metabolic Disease, Volume 48, Issue 6, November 2025.
ABSTRACT Tyrosine hydroxylase (TH) catalyses the rate‐limiting step in dopamine biosynthesis. Autosomal recessive tyrosine hydroxylase deficiency (THD) leads to clinical phenotypes reflecting the deficiency of dopamine, norepinephrine, or epinephrine in the central nervous system (CNS), presenting along a continuous spectrum from mild to severe forms ...
Mariya Sigatullina Bondarenko, Oya Kuseyri Hübschmann, Jan Kulhánek, Roser Pons, Toni S. Pearson, Kathrin Jeltsch, Ivana Badnjarevic, Tessa Wassenberg, Gabriella Horvath, Galina Stevanovic, Manju A. Kurian, Elisenda Cortès‐Saladelafont, Agathe Roubertie, Vincenzo Leuzzi, Mariarita Bertoldi, Mario Mastrangelo, Birgit Assmann, THD Guidelines Working Group, Ines Denzler, Clarisa Maxit, Natalia Alexandra Julia‐Palacios, Shekeeb Mohammad, Helly Goez, Wai‐Ian Yeung, Tomáš Honzík, Ivana Kavecan, Alba Tristán‐Noguero, Alberto Burlina, Daniela Gueraldi, Sushil Bandodkar, Willemsen Michel, Francesco Porta, Sheila Wong, Filippo Manti, Reem Alkhater, Chris Mühlhausen, Alice Kuster, Dimitrios Zafeiriou, Paulo Sgobbi, Wladimir Bocca Vieira de Rezende Pinto, Angeles Garcia‐Cazorla, Thomas Opladen   +41 more
wiley   +1 more source

Oculogyric Crisis During Treatment with Aripiprazole

, 2007
We report a case of oculogyric crisis (OGC) associated with aripiprazole (Abilify). Extrapyramidal symptoms (EPS), including oculogyric crisis (OGC), are side effects of neuroleptics, but rarely occur with newer partial dopamine and serotonin agonists ...
Erik Kobylarz; Nicholas Schiff; Jacqueline Winterkorn
core  

Tetrabenazine-induced oculogyric crisis – a rare complication in the treatment of Gilles de la Tourette syndrome

Neuropsychiatric Disease and Treatment, 2016
Piotr Janik,1 Monika Figura1,2 1Department of Neurology, Anna Gostynska Wolski Hospital, 2Department of Neurology, Faculty of Health Sciences, Medical University of Warsaw, Warsaw, Poland Abstract: Tetrabenazine is used in the treatment of chorea ...
Janik P, Figura M
doaj  

Oculogyric crisis as an initial manifestation of Wilson’s disease

Neurology, 1999
Wilson’s disease is an autosomal-recessive inherited disease caused by a defect on chromosome 13 encoding copper transporting P-type adenosine triphosphatase. Although patients with Wilson’s disease have a fundamental defect in the hepatobiliary system, they have various combinations of neurologic, psychiatric, and musculoskeletal manifestations.
M S, Lee, Y D, Kim, C H, Lyoo
openaire   +3 more sources

An Unusual Motor OFF in Parkinson's Disease

Movement Disorders Clinical Practice, Volume 13, Issue 4, Page 1085-1087, April 2026.
Shreyashi Jha, Mandar S. Jog
wiley   +1 more source

Rape Crisis Centre 1994 statistics and financial summary [PDF]

, 1995
I have audited the financial statements above and opposite in accordance with Auditing Standards. In my opinion, the financial statements give a true and fair view of the statement of the company's affairs at 31 st December 1994, and of its results ...
Rape Crisis Centre.
core