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	41.	Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation. [electronic resource] by Issa, Lina Mueller, Katrin Seufert, Katja Kraemer, Nadine Rosenkotter, Henning Ninnemann, Olaf Buob, Michael Kaindl, Angela M Morris-Rosendahl, Deborah J Producer: 20130723 In: Orphanet journal of rare diseases vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	Recessive mutation in EXOSC3 associates with mitochondrial dysfunction and pontocerebellar hypoplasia. [electronic resource] by Schottmann, Gudrun Picker-Minh, Sylvie Schwarz, Jana Marie Gill, Esther Rodenburg, Richard J T Stenzel, Werner Kaindl, Angela M Schuelke, Markus Producer: 20180619 In: Mitochondrion vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Many roads lead to primary autosomal recessive microcephaly. [electronic resource] by Kaindl, Angela M Passemard, Sandrine Kumar, Pavan Kraemer, Nadine Issa, Lina Zwirner, Angelika Gerard, Benedicte Verloes, Alain Mani, Shyamala Gressens, Pierre Producer: 20100615 In: Progress in neurobiology vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	Loss of CDK5RAP2 affects neural but not non-neural mESC differentiation into cardiomyocytes. [electronic resource] by Kraemer, Nadine Ravindran, Ethiraj Zaqout, Sami Neubert, Gerda Schindler, Detlev Ninnemann, Olaf Gräf, Ralph Seiler, Andrea E M Kaindl, Angela M Producer: 20160412 In: Cell cycle (Georgetown, Tex.) vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Genetic causes of MCPH in consanguineous Pakistani families. [electronic resource] by Kraemer, Nadine Picker-Minh, Sylvie Abbasi, Ansar A Fröhler, Sebastian Ninnemann, Olaf Khan, Muhammad N Ali, Ghazanfar Chen, Wei Kaindl, Angela M Producer: 20180709 In: Clinical genetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	Homozygous microdeletion of chromosome 4q11-q12 causes severe limb-girdle muscular dystrophy type 2E with joint hyperlaxity and contractures. [electronic resource] by Kaindl, Angela M Jakubiczka, Sibylle Lücke, Thomas Bartsch, Oliver Weis, Joachim Stoltenburg-Didinger, Gisela Aksu, Fuat Oexle, Konrad Koehler, Katrin Huebner, Angela Producer: 20060728 In: Human mutation vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	Comparative proteomics in neurodegenerative and non-neurodegenerative diseases suggest nodal point proteins in regulatory networking. [electronic resource] by Zabel, Claus Sagi, Dijana Kaindl, Angela M Steireif, Nicole Kläre, Yvonne Mao, Lei Peters, Hartmut Wacker, Maik A Kleene, Ralf Klose, Joachim Producer: 20070205 In: Journal of proteome research vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation. [electronic resource] by Farag, Heba Gamal Froehler, Sebastian Oexle, Konrad Ravindran, Ethiraj Schindler, Detlev Staab, Timo Huebner, Angela Kraemer, Nadine Chen, Wei Kaindl, Angela M Producer: 20140717 In: Orphanet journal of rare diseases vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	49.	Mice lacking the nuclear pore complex protein ALADIN show female infertility but fail to develop a phenotype resembling human triple A syndrome. [electronic resource] by Huebner, Angela Mann, Philipp Rohde, Elvira Kaindl, Angela M Witt, Martin Verkade, Paul Jakubiczka, Sibylle Menschikowski, Mario Stoltenburg-Didinger, Gisela Koehler, Katrin Producer: 20060404 In: Molecular and cellular biology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	50.	Identification of a novel homozygous TRAPPC9 gene mutation causing non-syndromic intellectual disability, speech disorder, and secondary microcephaly. [electronic resource] by Abbasi, Ansar A Blaesius, Kathrin Hu, Hao Latif, Zahid Picker-Minh, Sylvie Khan, Muhammad N Farooq, Sundas Khan, Muzammil A Kaindl, Angela M Producer: 20180216 In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 174 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	51.	Sedative and anticonvulsant drugs suppress postnatal neurogenesis. [electronic resource] by Stefovska, Vanya G Uckermann, Ortrud Czuczwar, Miroslaw Smitka, Martin Czuczwar, Piotr Kis, Jacek Kaindl, Angela M Turski, Lechoslaw Turski, Waldemar A Ikonomidou, Chrysanthy Producer: 20081224 In: Annals of neurology vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	52.	Diagnostic approach to microcephaly in childhood: a two-center study and review of the literature. [electronic resource] by von der Hagen, Maja Pivarcsi, Mark Liebe, Juliane von Bernuth, Horst Didonato, Nataliya Hennermann, Julia B Bührer, Christoph Wieczorek, Dagmar Kaindl, Angela M Producer: 20140912 In: Developmental medicine and child neurology vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	53.	Phenotype variability of infantile-onset multisystem neurologic, endocrine, and pancreatic disease IMNEPD. [electronic resource] by Picker-Minh, Sylvie Mignot, Cyril Doummar, Diane Hashem, Mais Faqeih, Eissa Josset, Patrice Dubern, Béatrice Alkuraya, Fowzan S Kraemer, Nadine Kaindl, Angela M Producer: 20171204 In: Orphanet journal of rare diseases vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	54.	Abnormal distribution of calcium-handling proteins: a novel distinctive marker in core myopathies. [electronic resource] by Herasse, Muriel Parain, Karine Marty, Isabelle Monnier, Nicole Kaindl, Angela M Leroy, Jean-Paul Richard, Pascale Lunardi, Jöel Romero, Norma B Ferreiro, Ana Producer: 20070215 In: Journal of neuropathology and experimental neurology vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	55.	Altered inhibition and excitation in neocortical circuits in congenital microcephaly. [electronic resource] by Zaqout, Sami Blaesius, Kathrin Wu, Yuan-Ju Ott, Stefanie Kraemer, Nadine Becker, Lena-Luise Rosário, Marta Rosenmund, Christian Strauss, Ulf Kaindl, Angela M Producer: 20200324 In: Neurobiology of disease vol. 129 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	56.	Synaptic NMDA receptor activity is coupled to the transcriptional control of the glutathione system. [electronic resource] by Baxter, Paul S Bell, Karen F S Hasel, Philip Kaindl, Angela M Fricker, Michael Thomson, Derek Cregan, Sean P Gillingwater, Thomas H Hardingham, Giles E Producer: 20160405 In: Nature communications vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	57.	Corrigendum: Synaptic NMDA receptor activity is coupled to the transcriptional control of the glutathione system. [electronic resource] by Baxter, Paul S Bell, Karen F S Hasel, Philip Kaindl, Angela M Fricker, Michael Thomson, Derek Cregan, Sean P Gillingwater, Thomas H Hardingham, Giles E Publication details: Nature communications 09 2017 In: Nature communications vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	58.	Dynamics of somatostatin type 2A receptor cargoes in living hippocampal neurons. [electronic resource] by Lelouvier, Benjamin Tamagno, Gianluca Kaindl, Angela M Roland, Alexandre Lelievre, Vincent Le Verche, Virginia Loudes, Catherine Gressens, Pierre Faivre-Baumann, Annie Lenkei, Zsolt Dournaud, Pascal Producer: 20080520 In: The Journal of neuroscience : the official journal of the Society for Neuroscience vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	59.	Implanted neurosphere-derived precursors promote recovery after neonatal excitotoxic brain injury. [electronic resource] by Titomanlio, Luigi Bouslama, Myriam Le Verche, Virginia Dalous, Jérémie Kaindl, Angela M Tsenkina, Yanina Lacaud, Adrien Peineau, Stéphane El Ghouzzi, Vincent Lelièvre, Vincent Gressens, Pierre Producer: 20110913 In: Stem cells and development vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	60.	Protection with estradiol in developmental models of apoptotic neurodegeneration. [electronic resource] by Asimiadou, Stiliani Bittigau, Petra Felderhoff-Mueser, Ursula Manthey, Daniela Sifringer, Marco Pesditschek, Stefanie Dzietko, Mark Kaindl, Angela M Pytel, Maria Studniarczyk, Dorota Mozrzymas, Jerzy W Ikonomidou, Chrysanthy Producer: 20051031 In: Annals of neurology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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