Movement Disorders (revue) - Exploration (Accueil)

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List of bibliographic references indexed by protein

Number of relevant bibliographic references: 46.
[20-40] [0 - 20][0 - 46][40-45][40-60]
Ident.Authors (with country if any)Title
001500 (2011) Michela Barichella [Italie] ; Carmen Madio [Italie] ; Erica Cassani [Italie] ; Cecilia Magris [Italie] ; Gianni Pezzoli [Italie]Oral high‐calorie, low‐protein supplements in a Parkinson's disease patient: A case report
001757 (2011) M. B. Aerts [Pays-Bas] ; R. A. J. Esselink [Pays-Bas] ; B. R. Bloem [Pays-Bas] ; M. M. Verbeek [Pays-Bas]Cerebrospinal fluid tau and phosphorylated tau protein are elevated in corticobasal syndrome
001835 (2011) Luca Errichiello [Italie] ; Marianna Pezzella [Italie] ; Lia Santulli [Italie] ; Salvatore Striano [Italie] ; Federico Zara [Italie] ; Carlo Minetti [Italie] ; Paolo Mainardi [Italie] ; Pasquale Striano [Italie]A proof‐of‐concept trial of the whey protein alfa‐lactalbumin in chronic cortical myoclonus
001839 (2011) Taku Hatano [Japon]A novel protein degradation system in young‐onset Parkinson's disease: Mitophagy is a therapeutic target as a quality control for damaged mitochondria
001968 (2010) William Dauer [États-Unis] ; Cherry Cheng-Ying Ho [États-Unis]The biology and pathology of the familial Parkinson's disease protein LRRK2
001A28 (2010) Kaori Nagasaka [Japon] ; Emiko Ohta [Japon] ; Takamura Nagasaka [Japon] ; Shinji Togashi [Japon] ; Michiaki Miwa [Japon] ; Yuki Nakamura [Japon] ; Kazumasa Shindo [Japon] ; Zenji Shiozawa [Japon]Rhythmic pupillary oscillation in Creutzfeldt‐Jakob disease associated with the Glu/Lys mutation of prion protein codon 200
001A81 (2010) Ana Maria Cuervo [États-Unis] ; Esther S. P. Wong [États-Unis] ; Marta Martinez-Vicente [États-Unis]Protein degradation, aggregation, and misfolding
001B92 (2010) Emanuele Cereda [Italie] ; Michela Barichella [Italie] ; Carlo Pedrolli [Italie] ; Gianni Pezzoli [Italie]Low‐protein and protein‐redistribution diets for Parkinson's disease patients with motor fluctuations: A systematic review
001E00 (2010) Kyoko Kanazawa [Japon] ; Satoko Kumada [Japon] ; Mitsuhiro Kato [Japon] ; Hirotomo Saitsu [Japon] ; Eiji Kurihara [Japon] ; Naomichi Matsumoto [Japon]Choreo–ballistic movements in a case carrying a missense mutation in syntaxin binding protein 1 gene
001E21 (2010) Josep Gamez [Espagne] ; Alba Sierra-Marcos [Espagne] ; Margarita Gratac S [Espagne] ; Laurade Jorge [Espagne] ; Nuria Raguer [Espagne] ; Dulce Moncho-Rodriguez [Espagne] ; Carlos Jacas [Espagne] ; Juan Conejero [Espagne] ; Merce Badia [Espagne] ; Carlos Lorenzo-Bosquet [Espagne] ; Victor Volpini [Espagne] ; Joan Castell-Conesa [Espagne]Camptocormia associated with an expanded allele in the TATA box‐binding protein gene
002029 (2009) John Depaolo [États-Unis] ; Ozlem Goker-Alpan [États-Unis] ; Ted Samaddar [États-Unis] ; Grisel Lopez [États-Unis] ; Ellen Sidransky [États-Unis]The association between mutations in the lysosomal protein glucocerebrosidase and parkinsonism
002312 (2009) Lina Shehadeh [États-Unis] ; Georgia Mitsi [États-Unis] ; Nikhil Adi [États-Unis] ; Nanette Bishopric [États-Unis] ; Spyridon Papapetropoulos [États-Unis]Expression of Lewy body protein septin 4 in postmortem brain of Parkinson's disease and control subjects
002F68 (2007) Ashish Nanda [États-Unis] ; Sarah A. Jackson [États-Unis] ; John D. Schwankhaus [États-Unis] ; W. Steven Metzer [États-Unis]Case of spinocerebellar ataxia type 17 (SCA17) associated with only 41 repeats of the TATA‐binding protein (TBP) gene
003187 (2006) Michela Barichella [Italie] ; Agnieszka Marczewska [Italie] ; Roberta De Notaris [Italie] ; Antonella Vairo [Italie] ; Cinzia Baldo [Italie] ; Andrea Mauri [Italie] ; Chiara Savardi [Italie] ; Gianni Pezzoli [Italie]Special low‐protein foods ameliorate postprandial off in patients with advanced Parkinson's disease
003238 (2006) Agnieszka Marczewska [Italie] ; Roberta De Notaris [Italie] ; Sabina Sieri [Italie] ; Michela Barichella [Italie] ; Elisabetta Fusconi [Italie] ; Gianni Pezzoli [Italie]Protein intake in Parkinsonian patients using the EPIC food frequency questionnaire
003D39 (2004) Dominic Thyagarajan [Australie] ; Timothy Chataway [Australie] ; Rong Li [États-Unis] ; Wei Ping Gai [Australie] ; Michael Brenner [États-Unis]Dominantly‐inherited adult‐onset leukodystrophy with palatal tremor caused by a mutation in the glial fibrillary acidic protein gene
004062 (2003) Masataka Nishimura [Japon] ; Sadako Kuno [Japon] ; Ikuko Mizuta [Japon] ; Mitsuhiro Ohta [Japon] ; Hirofumi Maruyama [Japon] ; Ryuji Kaji [Japon] ; Hideshi Kawakami [Japon]Influence of monocyte chemoattractant protein 1 gene polymorphism on age at onset of sporadic Parkinson's disease
004163 (2003) Demetrius M. Maraganore [États-Unis] ; Matthew J. Farrer [États-Unis] ; Timothy G. Lesnick [États-Unis] ; Mariza De Andrade [États-Unis] ; James H. Bower [États-Unis] ; Dena Hernandez [États-Unis] ; John A. Hardy [États-Unis] ; Walter A. Rocca [États-Unis]Case‐control study of the α‐synuclein interacting protein gene and Parkinson's disease
004285 (2002) Blas Morales ; Armando Martínez [Espagne] ; Isabel Gonzalo [Espagne] ; Lidice Vidal [Espagne] ; Raquel Ros [Espagne] ; Estrella Gomez-Tortosa [Espagne] ; Alberto Rabano [Espagne] ; Israel Ampuero [Espagne] ; Marina Sánchez [Espagne] ; Janet Hoenicka [Espagne] ; Justo García De Yébenes [Espagne]Steele‐Richardson‐Olszewski syndrome in a patient with a single C212Y mutation in the parkin protein
004344 (2002) Pauline L. Lee [États-Unis] ; Terri Gelbart [États-Unis] ; Carol West [États-Unis] ; Carol Halloran [États-Unis] ; Jack C. Sipe [États-Unis] ; Ernest Beutler [États-Unis]Polymorphisms in iron‐responsive binding protein 2 and lack of association with sporadic Parkinson's disease
004D17 (1999) Larry Baum [République populaire de Chine] ; Zhi-Ya Dong [République populaire de Chine] ; Ho-Keung Ng [République populaire de Chine] ; Lap Kay Law [République populaire de Chine] ; Jean Woo [République populaire de Chine] ; Chi Pui Pang [République populaire de Chine]Low‐density lipoprotein receptor‐related protein (LRP) gene 766T polymorphism and Parkinson's disease

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