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Author/Creator Steffann, J

1. A common pattern of brain MRI imaging in mitochondrial diseases with complex I deficiency. Issue 1 (23rd October 2010)

Authors:
Lebre, A S; Rio, M; Faivre d'Arcier, L; Vernerey, D; Landrieu, P; Slama, A; Jardel, C; Laforêt, P; Rodriguez, D; Dorison, N; Galanaud, D; Chabrol, B; Paquis-Flucklinger, V; Grévent, D; Edvardson, S; Steffann, J; Funalot, B; Villeneuve, N; Valayannopoulos, V; de Lonlay, P
Journal:
Journal of medical genetics
Issue:
Volume 48:Issue 1(2011)
Page Start:
16
Record Type:
Journal Article
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2. Analysis of mtDNA variant segregation during early human embryonic development: a tool for successful NARP preimplantation diagnosis. Issue 3 (9th September 2005)

Authors:
Steffann, J; Frydman, N; Gigarel, N; Burlet, P; Ray, P F; Fanchin, R; Feyereisen, E; Kerbrat, V; Tachdjian, G; Bonnefont, J-P; Frydman, R; Munnich, A
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 3(2006)
Page Start:
244
Record Type:
Journal Article
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5. P-553 Response to controlled ovarian stimulation and preimplantation genetic testing for molecular disease (PGT-M) outcomes for Myotonic dystrophy type I (DM1) : A French multicentric study. (30th June 2022)

Authors:
Sonigo, C; Ranisavljevic, N; Guigui, M; Anahory, T; Mayeur, A; Moutou, C; Rongières, C; Reignier, A; Lefebvre, T; Girardet, A; Ray, P; Steffann, J; Pirrello, O; Grynberg, M
Journal:
Human reproduction
Issue:
Volume 37(2022)Supplement 1
Page Start:
Record Type:
Journal Article
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7. Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal development. Issue 10 (11th May 2006)

Authors:
Bouchet, C; Steffann, J; Corcos, J; Monnot, S; Paquis, V; Rötig, A; Lebon, S; Levy, P; Royer, G; Giurgea, I; Gigarel, N; Benachi, A; Dumez, Y; Munnich, A; Bonnefont, J P
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 10(2006)
Page Start:
788
Record Type:
Journal Article
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8. Stability of the m.8993T→G mtDNA mutation load during human embryofetal development has implications for the feasibility of prenatal diagnosis in NARP syndrome. Issue 10 (1st June 2007)

Authors:
Steffann, J; Gigarel, N; Corcos, J; Bonnière, M; Encha-Razavi, F; Sinico, M; Prevot, S; Dumez, Y; Yamgnane, A; Frydman, R; Munnich, A; Bonnefont, J P
Journal:
Journal of medical genetics
Issue:
Volume 44:Issue 10(2007)
Page Start:
664
Record Type:
Journal Article
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9. The clinical utility of PGD with HLA matching: a collaborative multi-centre ESHRE study. Issue 3 (8th February 2018)

Authors:
Kakourou, G; Kahraman, S; Ekmekci, G C; Tac, H A; Kourlaba, G; Kourkouni, E; Sanz, A Cervero; Martin, J; Malmgren, H; Giménez, C; Gold, V; Carvalho, F; Billi, C; Chow, J F C; Vendrell, X; Kokkali, G; Liss, J; Steffann, J; Traeger-Synodinos, J
Journal:
Human reproduction
Issue:
Volume 33:Issue 3(2018)
Page Start:
520
Record Type:
Journal Article
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10. What is the threshold of mature oocytes to obtain at least one healthy transferable cleavage-stage embryo after preimplantation genetic testing for fragile X syndrome?. Issue 11 (26th September 2021)

Authors:
Sonigo, C; Mayeur, A; Sadoun, M; Pinto, M; Benguigui, J; Frydman, N; Monnot, S; Benachi, A; Steffann, J; Grynberg, M
Journal:
Human reproduction
Issue:
Volume 36:Issue 11(2021)
Page Start:
3003
Record Type:
Journal Article
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