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Sexually Transmitted Diseases, ISSN 0148-5717, 06/2019
OBJECTIVESTo compare molecular and epidemiological differences between ceftriaxone reduced susceptible (CRO-RS) and ceftriaxone susceptible (CRO-S) Neisseria... 
Journal Article
Nature biotechnology, ISSN 1087-0156, 2014, Volume 32, Issue 10, pp. 1019 - 1025
Journal Article
Nature Neuroscience, ISSN 1097-6256, 03/2016, Volume 19, Issue 3, p. 494
Although genome sequencing has identified numerous noncoding alterations between primate species, which of those are regulatory and potentially relevant to the... 
Journal Article
Nature Neuroscience, ISSN 1097-6256, 03/2016, Volume 9, Issue 3, p. 494–503
Although genome sequencing has identified numerous noncoding alterations between primate species, which of those are regulatory and potentially relevant to the... 
Journal Article
Genes and Development, ISSN 0890-9369, 09/2016, Volume 30, Issue 17, p. 1937
Sequential 3′-to-5′ activation of the Hox gene clusters in early embryos is a most fascinating issue in developmental biology. Neither the trigger nor the... 
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2010, Volume 56, Issue 8, pp. 617 - 626
Journal Article
Journal Article
BBA Clinical, ISSN 2214-6474, 12/2016, Volume 6, pp. 19 - 24
The m.3243A > G mutation is the most prevalent, disease-causing mitochondrial DNA (mtDNA) mutation. In a national cohort study of 48 families harbouring the... 
Mitochondrial myopathy, encephalopathy, lactate acidosis and stroke-like episodes (MELAS) | Maternally inherited diabetes and deafness (MIDD) | Genetic counselling | m.3243A > G mutation | Inheritance | M.3243A > G mutation
Journal Article
Cell Reports [E], ISSN 2211-1247, 2014, Volume 9, Issue 2, p. 767
Understanding the complexity of the human brain and its functional diversity remain a major challenge. Distinct anatomical regions are involved in an array of... 
Journal Article
Neuroendocrinology, ISSN 0028-3835, 2012, Volume 96, pp. 25 - 25
Journal Article
Otology & Neurotology, ISSN 1531-7129, 06/2018, Volume 39, Issue 5, pp. 648 - 653
OBJECTIVES:Finding the underlying cause for pulsatile tinnitus can be challenging. We aimed to determine the incidence of arteriovenous shunts, i.e.,... 
Clinical features | Tinnitus | Angiography | Dural arteriovenous fistula | Arteriovenous malformation | OTORHINOLARYNGOLOGY | CLASSIFICATION | COMPLICATION RATE | CLINICAL NEUROLOGY | Development and progression | Care and treatment | Usage | Arteriovenous shunts, Surgical | Health aspects
Journal Article
ORPHANET JOURNAL OF RARE DISEASES, ISSN 1750-1172, 05/2017, Volume 12
Background: More than half of the patients harbouring the m. 3243A > G mutation were found to have trouble maintaining balance when walking in a recent study... 
MEDICINE, RESEARCH & EXPERIMENTAL | Trial | Gait | OLDER-ADULTS | DISORDERS | CLASSIFICATION | Mitochondrial disease | VARIABILITY | M.3243A-GREATER-THAN-G | MUTATION | GENETICS & HEREDITY | MELAS | m. 3243A > G | PARKINSONS-DISEASE
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2017, Volume 12, Issue 1, pp. 91 - 9
Journal Article
by Maffioletti, S M and Sarcar, S and Henderson, A and Mannhardt, I and Pinton, L and Moyle, L A and Moyle, L A and Steele-Stallard, H and Cappellari, O and Wells, K E and Ragazzi, M and Ragazzi, M and Ragazzi, M and Wang, W and Wang, W and Zammit, P and Wells, D J and Eschenhagen, T and Jung-Klawitter, S and Fuchs, N V and Upton, K R and Frömmrich, A and Miskey, C and Muñoz-Lopez, M and Shukla, R and Wang, J and Sebe, A and Merkert, S and Bock, A and Held, U and Menzel, M and Gogol-Döring, A and Haase, A and Izsvák, Z and Izsvák, Z and Ivics, Z and Martin, U and Garcia-Perez, J and Faulkner, G J and Terrasso, A P and Silva, M M and Arez, F and Sousa, M F and Raimundo, N and Gomes-Alves, P and Kremer, E J and Alves, P M and Brito, C and Moser, R and Decembrini, S and Gamm, D and Gamm, D and de Leone, V Ponce and Alves, S and Christaller, W and Subashi, E and Kacher, R and Lamazière, A and Despres, G and Saudou, F and Caboche, J and Betuing, S and Miyauchi, A and Nakajima, T and Taga, N and Ono, S A and Mizukami, H and Kato, M and Osaka, H and Muramatsu, S and Yamagata, T and Bouquet, C and Pruneau, D and Pruneau, D and Thomasson, N and Thomasson, N and Chavas, J and Chavas, J and Galluppi, F and Dalkara, D and Besnosman, R and Chenegros, G and Picaud, S and Sahel, J and Massó, A and Sánchez, A and Bosch, A and Blanch, R and Espinosa, J F and Giménez-Llort, L and Heidbüchel, J and Veinalde, R and Veinalde, R and Veinalde, R and Jäger, D and Jäger, D and Jäger, D and von Kalle, C and von Kalle, C and von Kalle, C and ...
Human Gene Therapy, ISSN 1043-0342, 12/2017, Volume 28, Issue 12, pp. A1 - A125
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2016, Volume 11
BACKGROUND: Mitochondrial disorders belong to the most prevalent inherited metabolic diseases with the m.3243A > G mutation reflecting being one of the most... 
Journal Article
Journal Article