Lorenzo Sanz G - Search Results

1

[Septo-optic dysplasia: absence of the hypophysial stalk in the MRI image].

Ramos Fernández JM, Barrio Castellanos R, Yturriaga Matarranz R, Lorenzo Sanz G, de Miguel Durán F, Aparicio Meix JM. Ramos Fernández JM, et al. Among authors: lorenzo sanz g. An Esp Pediatr. 1992 Oct;37(4):324-6. An Esp Pediatr. 1992. PMID: 1443945 Spanish. No abstract available.

2

[Severe bone malformations in fetal valproic acid disease].

Lorenzo Sanz G, Serna Saugar C, Quintana Castilla A, Lozano Giménez C, Aparicio Meix JM. Lorenzo Sanz G, et al. An Esp Pediatr. 1993 Jul;39(1):19-21. An Esp Pediatr. 1993. PMID: 8363144 Spanish.

3

[The Robinow syndrome: a report of a family with autosomal dominant transmission].

Díaz López MT, Lorenzo Sanz G, Quintana Castilla A, Esteve de Pablo C, Aparicio Meix JM. Díaz López MT, et al. Among authors: lorenzo sanz g. An Esp Pediatr. 1996 May;44(5):520-3. An Esp Pediatr. 1996. PMID: 8928981 Review. Spanish. No abstract available.

4

[Septo-optic dysplasia: report of 6 patients studied with MR and discussion on its pathogenesis].

Ramos Fernández JM, Martínez San Millán J, Barrio Castellano R, Yturriaga Matarranz R, Lorenzo Sanz G, Aparicio Meix JM. Ramos Fernández JM, et al. Among authors: lorenzo sanz g. An Esp Pediatr. 1996 Dec;45(6):614-8. An Esp Pediatr. 1996. PMID: 9133227 Spanish.

5

[Spinocerebellar syndrome of early onset associated with retinal degeneration. Report of a case].

Onsurbe Ramírez I, Lorenzo Sanz G, Aparicio Meix JM. Onsurbe Ramírez I, et al. Among authors: lorenzo sanz g. An Esp Pediatr. 1990 Oct;33(4):387-9. An Esp Pediatr. 1990. PMID: 2278445 Spanish. No abstract available.

6

[Autosomal recessive limb-girdle muscular dystrophy probably linked to chromosome 15].

Noguera Moya A, Lorenzo Sanz G, García Villanueva M, Benítez J, Aparicio Méix JM. Noguera Moya A, et al. Among authors: lorenzo sanz g. An Esp Pediatr. 1996 Mar;44(3):267-9. An Esp Pediatr. 1996. PMID: 8830604 Review. Spanish. No abstract available.

7

[Acute intermittent familial ataxia: report of a new family].

Pérez-Rodríguez MJ, Lorenzo-Sanz G, Aparicio-Meix JM. Pérez-Rodríguez MJ, et al. Among authors: lorenzo sanz g. Rev Neurol. 1996 May;24(129):570-1. Rev Neurol. 1996. PMID: 8681177 Spanish.

8

[Focal myositis: report of a case in pediatric age and review of the literature].

Lorenzo-Sanz G, Egea-Nadal P, García-Villanueva M, Gamir ML, Ocete G, García-Lacalle C. Lorenzo-Sanz G, et al. Rev Neurol. 1998 Sep;27(157):505-8. Rev Neurol. 1998. PMID: 9774828 Review. Spanish.

9

Bone Infarct as an Indicator of Acute Spinal Ischaemia.

López-Viñas L, Quiñones-Coneo KL, Buenache-Espartosa R, Martínez-San-Millán JS, Lorenzo-Sanz G. López-Viñas L, et al. Among authors: lorenzo sanz g. Case Rep Pediatr. 2020 Feb 26;2020:9703625. doi: 10.1155/2020/9703625. eCollection 2020. Case Rep Pediatr. 2020. PMID: 32181041 Free PMC article.

10

[Type C hereditary brachydactyly].

Lorenzo Sanz G, Barrios Castellanos R, Quintana Castilla A, Corbatón Blasco J, García Lacalle C. Lorenzo Sanz G, et al. Rev Clin Esp. 1989 Feb;184(3):139-42. Rev Clin Esp. 1989. PMID: 2717793 Spanish.

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