Sturtz F - Search Results

1

[Hereditary motor and sensory neuropathy of Charcot-Marie-Tooth disease].

Sturtz F, Gonnaud PM, Besse JL, Chazot G, Vandenberghe A. Sturtz F, et al. Arch Pediatr. 1995 Jan;2(1):70-8. doi: 10.1016/0929-693x(96)89813-7. Arch Pediatr. 1995. PMID: 7735430 Review. French.

2

Netazepide, an Antagonist of Cholecystokinin Type 2 Receptor, Prevents Vincristine-Induced Sensory Neuropathy in Mice.

Bernard A, Mroué M, Bourthoumieu S, Boyce M, Richard L, Sturtz F, Demiot C, Danigo A. Bernard A, et al. Among authors: sturtz f. Pharmaceuticals (Basel). 2024 Jan 23;17(2):144. doi: 10.3390/ph17020144. Pharmaceuticals (Basel). 2024. PMID: 38399359 Free PMC article.

3

Neuroprotective Effect of Polyvalent Immunoglobulins on Mouse Models of Chemotherapy-Induced Peripheral Neuropathy.

Mroué M, Bessaguet F, Nizou A, Richard L, Sturtz F, Magy L, Bourthoumieu S, Danigo A, Demiot C. Mroué M, et al. Among authors: sturtz f. Pharmaceutics. 2024 Jan 20;16(1):139. doi: 10.3390/pharmaceutics16010139. Pharmaceutics. 2024. PMID: 38276509 Free PMC article.

4

[Reversible retroperitoneal fibrosis after prolonged treatment with bromocriptine: apropos of 2 cases].

Dupuis J, Bodnar D, Sturtz F, Broussolle E, Exbrayat C, Lapras V, Chazot G. Dupuis J, et al. Among authors: sturtz f. Rev Med Interne. 1990 Mar-Apr;11(2):183. doi: 10.1016/s0248-8663(05)82228-3. Rev Med Interne. 1990. PMID: 2399383 French. No abstract available.

5

Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP).

Le Guern E, Sturtz F, Gugenheim M, Gouider R, Bonnebouche C, Ravisé N, Gonnaud PM, Tardieu S, Bouche P, Chazot G, et al. Le Guern E, et al. Among authors: sturtz f. Cytogenet Cell Genet. 1994;65(4):261-4. doi: 10.1159/000133643. Cytogenet Cell Genet. 1994. PMID: 7903071

6

X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 gene.

Ressot C, Latour P, Blanquet-Grossard F, Sturtz F, Duthel S, Battin J, Corbillon E, Ollagnon E, Serville F, Vandenberghe A, Dautigny A, Pham-Dinh D. Ressot C, et al. Among authors: sturtz f. Hum Genet. 1996 Aug;98(2):172-5. doi: 10.1007/s004390050183. Hum Genet. 1996. PMID: 8698335

7

Modelization of motor nerve conduction velocities for Charcot-Marie-Tooth (Type-1) patients. CMT-France Network.

Sturtz FG, Chauvin F, Ollagnon-Roman E, Bost M, Latour P, Bonnebouche C, Gonnaud PM, Bady B, Chazot G, Vandenberghe A. Sturtz FG, et al. Eur Neurol. 1996;36(4):224-8. doi: 10.1159/000117254. Eur Neurol. 1996. PMID: 8814426

8

DNA analysis as a tool to confirm the diagnosis of asymptomatic hereditary neuropathy with liability to pressure palsies (HNPP) with further evidence for the occurrence of de novo mutations.

Gonnaud PM, Sturtz F, Fourbil Y, Bonnebouche C, Tranchant C, Warter JM, Chazot G, Bady B, Vial C, Brechard AS, et al. Gonnaud PM, et al. Among authors: sturtz f. Acta Neurol Scand. 1995 Oct;92(4):313-8. doi: 10.1111/j.1600-0404.1995.tb00135.x. Acta Neurol Scand. 1995. PMID: 8848937

9

New mutations in the X-linked form of Charcot-Marie-Tooth disease.

Latour P, Fabreguette A, Ressot C, Blanquet-Grossard F, Antoine JC, Calvas P, Chapon F, Corbillon E, Ollagnon E, Sturtz F, Boucherat M, Chazot G, Dautigny A, Pham-Dinh D, Vandenberghe A. Latour P, et al. Among authors: sturtz f. Eur Neurol. 1997;37(1):38-42. doi: 10.1159/000117403. Eur Neurol. 1997. PMID: 9018031 Review.

10

Clinical and electrophysiological phenotype of a homozygously duplicated Charcot-Marie-Tooth (type 1A) disease.

Sturtz FG, Latour P, Mocquard Y, Cruz S, Fenoll B, LeFur JM, Mabin D, Chazot G, Vandenberghe A. Sturtz FG, et al. Eur Neurol. 1997;38(1):26-30. doi: 10.1159/000112898. Eur Neurol. 1997. PMID: 9252795

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