Touati G - Search Results

1

Liver hepatoblastoma and multiple OXPHOS deficiency in the follow-up of a patient with methylmalonic aciduria.

Cosson MA, Touati G, Lacaille F, Valayannnopoulos V, Guyot C, Guest G, Verkarre V, Chrétien D, Rabier D, Munnich A, Benoist JF, de Keyzer Y, Niaudet P, de Lonlay P. Cosson MA, et al. Among authors: touati g. Mol Genet Metab. 2008 Sep-Oct;95(1-2):107-9. doi: 10.1016/j.ymgme.2008.06.007. Epub 2008 Aug 3. Mol Genet Metab. 2008. PMID: 18676166

2

[Hereditary metabolic diseases in adults].

Saudubray JM, Nuoffer JM, de Lonlay P, Castelnau P, Touati G. Saudubray JM, et al. Among authors: touati g. Rev Med Interne. 1998;19 Suppl 3:366S-375S. Rev Med Interne. 1998. PMID: 9885858 Review. French. No abstract available.

3

Recognition and management of fatty acid oxidation defects: a series of 107 patients.

Saudubray JM, Martin D, de Lonlay P, Touati G, Poggi-Travert F, Bonnet D, Jouvet P, Boutron M, Slama A, Vianey-Saban C, Bonnefont JP, Rabier D, Kamoun P, Brivet M. Saudubray JM, et al. Among authors: touati g. J Inherit Metab Dis. 1999 Jun;22(4):488-502. doi: 10.1023/a:1005556207210. J Inherit Metab Dis. 1999. PMID: 10407781 Review.

4

Liver transplantation in urea cycle disorders.

Saudubray JM, Touati G, Delonlay P, Jouvet P, Narcy C, Laurent J, Rabier D, Kamoun P, Jan D, Revillon Y. Saudubray JM, et al. Among authors: touati g. Eur J Pediatr. 1999 Dec;158 Suppl 2:S55-9. doi: 10.1007/pl00014323. Eur J Pediatr. 1999. PMID: 10603100

5

Liver transplantation in propionic acidaemia.

Saudubray JM, Touati G, Delonlay P, Jouvet P, Schlenzig J, Narcy C, Laurent J, Rabier D, Kamoun P, Jan D, Revillon Y. Saudubray JM, et al. Among authors: touati g. Eur J Pediatr. 1999 Dec;158 Suppl 2:S65-9. doi: 10.1007/pl00014325. Eur J Pediatr. 1999. PMID: 10603102

6

Dietary therapy in two patients with a mild form of sulphite oxidase deficiency. Evidence for clinical and biological improvement.

Touati G, Rusthoven E, Depondt E, Dorche C, Duran M, Heron B, Rabier D, Russo M, Saudubray JM. Touati G, et al. J Inherit Metab Dis. 2000 Feb;23(1):45-53. doi: 10.1023/a:1005646813492. J Inherit Metab Dis. 2000. PMID: 10682307

7

Genetic hypoglycaemia in infancy and childhood: pathophysiology and diagnosis.

Saudubray JM, de Lonlay P, Touati G, Martin D, Nassogne MC, Castelnau P, Sevin C, Laborde C, Baussan C, Brivet M, Vassault A, Rabier D, Bonnefont JP, Kamoun P. Saudubray JM, et al. Among authors: touati g. J Inherit Metab Dis. 2000 May;23(3):197-214. doi: 10.1023/a:1005675827612. J Inherit Metab Dis. 2000. PMID: 10863937 Review. No abstract available.

8

Neurologic outcomes of 90 neonates and infants with persistent hyperinsulinemic hypoglycemia.

Menni F, de Lonlay P, Sevin C, Touati G, Peigné C, Barbier V, Nihoul-Fékété C, Saudubray JM, Robert JJ. Menni F, et al. Among authors: touati g. Pediatrics. 2001 Mar;107(3):476-9. doi: 10.1542/peds.107.3.476. Pediatrics. 2001. PMID: 11230585

9

Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomatic carrier with 'de novo' duplication of dystrophin gene.

Romero NB, De Lonlay P, Llense S, Leturcq F, Touati G, Urtizberea JA, Saudubray JM, Munnich A, Kaplan JC, Récan D. Romero NB, et al. Among authors: touati g. Neuromuscul Disord. 2001 Jul;11(5):494-8. doi: 10.1016/s0960-8966(01)00192-4. Neuromuscul Disord. 2001. PMID: 11404124

10

Hyperinsulinism and hyperammonemia syndrome: report of twelve unrelated patients.

De Lonlay P, Benelli C, Fouque F, Ganguly A, Aral B, Dionisi-Vici C, Touati G, Heinrichs C, Rabier D, Kamoun P, Robert JJ, Stanley C, Saudubray JM. De Lonlay P, et al. Among authors: touati g. Pediatr Res. 2001 Sep;50(3):353-7. doi: 10.1203/00006450-200109000-00010. Pediatr Res. 2001. PMID: 11518822

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