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Author/Creator Polak, Michel

2. A novel NEUROG3 mutation in neonatal diabetes associated with a neuro‐intestinal syndrome. Issue 3 (22nd September 2017)

Authors:
Hancili, Suna; Bonnefond, Amélie; Philippe, Julien; Vaillant, Emmanuel; De Graeve, Franck; Sand, Olivier; Busiah, Kanetee; Robert, Jean‐Jacques; Polak, Michel; Froguel, Philippe; Güven, Ayla; Vaxillaire, Martine
Journal:
Pediatric diabetes
Issue:
Volume 19:Issue 3(2018)
Page Start:
381
Record Type:
Journal Article
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3. Analysis of a pitfall in congenital adrenal hyperplasia newborn screening: evidence of maternal use of corticoids detected on dried blood spot. Issue 6 (15th June 2022)

Authors:
Houang, Muriel; Nguyen-Khoa, Thao; Eguether, Thibaut; Ribault, Bettina; Brabant, Séverine; Polak, Michel; Netchine, Irène; Lamazière, Antonin
Journal:
Endocrine connections
Issue:
Volume 11:Issue 6(2022)
Page Start:
Record Type:
Journal Article
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4. Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene. Issue 10 (24th July 2012)

Authors:
Gras, Domitille; Jonard, Laurence; Roze, Emmanuel; Chantot-Bastaraud, Sandra; Koht, Jeanette; Motte, Jacques; Rodriguez, Diana; Louha, Malek; Caubel, Isabelle; Kemlin, Isabelle; Lion-François, Laurence; Goizet, Cyril; Guillot, Loic; Moutard, Marie-Laure; Epaud, Ralph; Héron, Bénédicte; Charles, P...
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 83:Issue 10(2012)
Page Start:
956
Record Type:
Journal Article
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5. Bone Health Should Be an Important Concern in the Care of Patients Affected by 21 Hydroxylase Deficiency. (21st September 2010)

Authors:
Bachelot, Anne; Chakhtoura, Zeina; Samara-Boustani, Dinane; Dulon, Jérome; Touraine, Philippe; Polak, Michel
Other Names:
Fuqua John Academic Editor.
Journal:
International journal of pediatric endocrinology
Issue:
Volume 2010(2010)
Page Start:
Record Type:
Journal Article
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6. Bone Health Should Be an Important Concern in the Care of Patients Affected by 21 Hydroxylase Deficiency. (21st September 2010)

Authors:
Bachelot, Anne; Chakhtoura, Zeina; Samara-Boustani, Dinane; Dulon, Jérome; Touraine, Philippe; Polak, Michel
Other Names:
Fuqua John Academic Editor.
Journal:
International journal of pediatric endocrinology
Issue:
Volume 2010(2010)
Page Start:
Record Type:
Journal Article
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8. Clinical and biological characterization of 20 patients with TANGO2 deficiency indicates novel triggers of metabolic crises and no primary energetic defect. Issue 2 (28th September 2020)

Authors:
Bérat, Claire‐Marine; Montealegre, Sebastian; Wiedemann, Arnaud; Nuzum, Malou Le Corronc; Blondel, Amélie; Debruge, Hugo; Cano, Aline; Chabrol, Brigitte; Hoebeke, Célia; Polak, Michel; Stoupa, Athanasia; Feillet, François; Torre, Stéphanie; Boddaert, Nathalie; Bruel, Henri; Barth, Magalie; Damaj,...
Journal:
Journal of inherited metabolic disease
Issue:
Volume 44:Issue 2(2021)
Page Start:
415
Record Type:
Journal Article
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9. Clinical characteristics and genotype‐phenotype correlations of 130 Chinese children in a high‐homogeneity single‐center cohort with 5α‐reductase 2 deficiency. Issue 10 (26th July 2020)

Authors:
Fan, Lijun; Song, Yanning; Polak, Michel; Li, Lele; Ren, Xiaoya; Zhang, Beibei; Wu, Di; Gong, Chunxiu
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 8:Issue 10(2020)
Page Start:
n/a
Record Type:
Journal Article
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10. Clinical characteristics, growth patterns, and long‐term diabetes complications of 24 patients with neonatal diabetes mellitus: A single center experience. Issue 1 (6th December 2021)

Authors:
Mouler, Marie; Lebenthal, Yael; de Vries, Liat; Yackobovitch‐Gavan, Michal; Averbuch, Noa Shefer; Fauret‐Amsellem, Anne Laure; Cavé, Helene; Beltrand, Jacques; Polak, Michel; Phillip, Moshe; Nimri, Revital
Journal:
Pediatric diabetes
Issue:
Volume 23:Issue 1(2022)
Page Start:
45
Record Type:
Journal Article
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