Ga doping induced thermal stabilization of fcc phase in Ge2Sb2Te5 thin films: A step toward power-efficient phase change memories von Bala, Neeru, Goutam, U. K., Thakur, Anup

Volltext

The genetic landscape of the epileptic encephalopathies of infancy and childhood von McTague, Amy, MBChB, Howell, Katherine B, MBBS, Cross, J Helen, Prof, Kurian, Manju A, PhD, Scheffer, Ingrid E, Prof

Volltext

Plant Physiology, Development and Metabolism von Bhatla, Satish C

Volltext

Nanotechnology-Assisted Metered-Dose Inhalers (MDIs) for High-Performance Pulmonary Drug Delivery Applications von Kumar, Raj, Mehta, Piyush, Shankar, Konathala Ravi, Rajora, Manju A. K., Mishra, Yogendra Kumar, Mostafavi, Ebrahim, Kaushik, Ajeet

Volltext

Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA von Haack, Tobias B., Hogarth, Penelope, Kruer, Michael C., Gregory, Allison, Wieland, Thomas, Schwarzmayr, Thomas, Graf, Elisabeth, Sanford, Lynn, Meyer, Esther, Kara, Eleanna, Cuno, Stephan M., Harik, Sami I., Dandu, Vasuki H., Nardocci, Nardo, Zorzi, Giovanna, Dunaway, Todd, Tarnopolsky, Mark, Skinner, Steven, Frucht, Steven, Hanspal, Era, Schrander-Stumpel, Connie, Héron, Delphine, Mignot, Cyril, Garavaglia, Barbara, Bhatia, Kailash, Hardy, John, Strom, Tim M., Boddaert, Nathalie, Houlden, Henry H., Kurian, Manju A., Meitinger, Thomas, Prokisch, Holger, Hayflick, Susan J.

Volltext

The role of manganese dysregulation in neurological disease: emerging evidence von Budinger, Dimitri, Barral, Serena, Soo, Audrey K S, Kurian, Manju A

Volltext

An Update on the Phenotype, Genotype and Neurobiology of ADCY5‐Related Disease von Ferrini, Arianna, Steel, Dora, Barwick, Katy, Kurian, Manju A.

Volltext

Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms von Abela, Lucia, Kurian, Manju A.

Volltext

The Impact of Restricting Labor Mobility on Corporate Investment and Entrepreneurship von Jeffers, Jessica S

Volltext

Optimizing long chain-polyunsaturated fatty acid synthesis in salmonids by balancing dietary inputs von Colombo, Stefanie M, Parrish, Christopher C, Wijekoon, Manju P A

Volltext

Applications of quantum inspired computational intelligence: a survey von Manju, A., Nigam, M. J.

Volltext

The expanding spectrum of movement disorders in genetic epilepsies von Papandreou, Apostolos, Danti, Federica Rachele, Spaull, Robert, Leuzzi, Vincenzo, Mctague, Amy, Kurian, Manju A

Volltext

Gene Therapy for Dopamine Dyshomeostasis: From Parkinson's to Primary Neurotransmitter Diseases von Ng, Joanne, Barral, Serena, Waddington, Simon N., Kurian, Manju A.

Volltext

HOPS-associated neurological disorders (HOPSANDs): linking endolysosomal dysfunction to the pathogenesis of dystonia von Monfrini, Edoardo, Zech, Michael, Steel, Dora, Kurian, Manju A, Winkelmann, Juliane, Di Fonzo, Alessio

Volltext

Exome Sequence Reveals Mutations in CoA Synthase as a Cause of Neurodegeneration with Brain Iron Accumulation von Dusi, Sabrina, Valletta, Lorella, Haack, Tobias B., Tsuchiya, Yugo, Venco, Paola, Pasqualato, Sebastiano, Goffrini, Paola, Tigano, Marco, Demchenko, Nikita, Wieland, Thomas, Schwarzmayr, Thomas, Strom, Tim M., Invernizzi, Federica, Garavaglia, Barbara, Gregory, Allison, Sanford, Lynn, Hamada, Jeffrey, Bettencourt, Conceição, Houlden, Henry, Chiapparini, Luisa, Zorzi, Giovanna, Kurian, Manju A., Nardocci, Nardo, Prokisch, Holger, Hayflick, Susan, Gout, Ivan, Tiranti, Valeria

Volltext

Correction: Nanotechnology-Assisted Metered-Dose Inhalers (MDIs) for High-Performance Pulmonary Drug Delivery Applications von Kumar, Raj, Mehta, Piyush, Shankar, Konathala Ravi, Rajora, Manju A. K., Mishra, Yogendra Kumar, Mostafavi, Ebrahim, Kaushik, Ajeet

Volltext

The monoamine neurotransmitter disorders: an expanding range of neurological syndromes von Kurian, Manju A, Dr, Gissen, Paul, PhD, Smith, Martin, PhD, Heales, Simon JR, Prof, Clayton, Peter T, Prof

Volltext

Freeze! Financial Sanctions and Bank Responses von Efing, Matthias, Goldbach, Stefan, Nitsch, Volker

Volltext

Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis von Trump, Natalie, McTague, Amy, Brittain, Helen, Papandreou, Apostolos, Meyer, Esther, Ngoh, Adeline, Palmer, Rodger, Morrogh, Deborah, Boustred, Christopher, Hurst, Jane A, Jenkins, Lucy, Kurian, Manju A, Scott, Richard H

Volltext

The clinical and genetic heterogeneity of paroxysmal dyskinesias von Gardiner, Alice R, Jaffer, Fatima, Dale, Russell C, Labrum, Robyn, Erro, Roberto, Meyer, Esther, Xiromerisiou, Georgia, Stamelou, Maria, Walker, Matthew, Kullmann, Dimitri, Warner, Tom, Jarman, Paul, Hanna, Mike, Kurian, Manju A, Bhatia, Kailash P, Houlden, Henry

Volltext