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J LAFOURCADE

Explore the profile of J LAFOURCADE including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 89
Citations 472
Followers 0
Related Specialties
Pediatrics
General Medicine
Genetics
Top 10 Co-Authors
J LeJeune
R TURPIN
J Cruveiller
M O Rethore
B Caille
R Berger
J P Harpey
B Dutrillaux
R Gorin
L Bocquet
Published In
Ann Genet
Arch Fr Pediatr
Ann Pediatr (Paris)
Sem Hop
Rev Prat
Affiliations
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Recent Articles
1.
Infectious mononucleosis; Lichenoid papular rash; skin biopsy
CELICE J, GROSSIORD A, LAFOURCADE J
Bull Mem Soc Med Hop Paris . 2010 Oct; 62(15-17):281-3. PMID: 20991277
No abstract available.
2.
Familial aggregation of malignant melanoma/dysplastic naevi and tumours of the nervous system: an original syndrome of tumour proneness
Bahuau M, Vidaud D, Kujas M, Palangie A, Assouline B, PRIEUR M, et al.
Ann Genet . 1997 Jan; 40(2):78-91. PMID: 9259954
A five-generation family is here reported in which several members developed malignant melanoma, dysplastic naevi, astrocytoma in all grades, benign or malignant schwannoma, neurofibroma, or meningioma in a single instance....
3.
[Successful separation in 1974 of craniopagus twins united at the vertex. Indications, technics, follow-up after 14 years]
PERTUISET B, LAFOURCADE J, VIARS P, Nicoletis C, Metzger J, Ancri D, et al.
Neurochirurgie . 1989 Jan; 35(3):177-85. PMID: 2622518
On July 22, 1974, 55 days after delivery, the separation of female craniopagus twins united at the vertex was performed. This case was very similar to the case published by...
4.
[17p trisomy]
Rethore M, Renault F, LAFOURCADE J, Supeira C, Padovani J, LeJeune J
Sem Hop . 1983 Jul; 59(27-28):2039-42. PMID: 6312571
Trisomy 17p resulting from a parental translocation t(10;17)(q26.3;p11) was observed in a 22-month-old boy. Analysis of five cases of trisomy 17p from the literature indicates a common malformation pattern: microcephaly,...
5.
[A case report on a familial incidence of tumors]
Caille B, LAFOURCADE J
J Genet Hum . 1983 Mar; 31(1):13-4. PMID: 6619805
No abstract available.
6.
[Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat]
Rethore M, LAFOURCADE J, Couturier J, Harpey J, Hamet M, Engler R, et al.
Sem Hop . 1982 Dec; 58(45):2639-45. PMID: 6297060
Two cousins with trisomy for the distal third of 16q due to a familial translocation, t(16;21)(q22.2;q22.2), are reported. The APRT gene locus could be assigned to 16q22.2 to 16qter. The...
7.
[Larsen's syndrome. Clinical findings and inheritance (author's transl)]
Renault F, Arthuis M, Rethore M, LAFOURCADE J
Arch Fr Pediatr . 1982 Jan; 39(1):35-8. PMID: 7065820
Three new case reports of Larsen's syndrome (multiple congenital dislocations of the joints, distinctive facies and skeletal abnormalities) are presented. For the first time this condition is described to be...
8.
[X chromosome fragility and effects of trimethoprim]
LeJeune J, Legrand N, LAFOURCADE J, Rethore M, Raoul O, Maunoury C
Ann Genet . 1982 Jan; 25(3):149-51. PMID: 6982662
Severe clinical regression was observed in a patient carrier of a fragile X after treatment trimethoprime. This prompted us to examine the effect of this antibiotic in lymphocyte cultures: a...
9.
[Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat (author's transl)]
Rethore M, LAFOURCADE J, Couturier J, Harpey J, Hamet M, Engler R, et al.
Ann Genet . 1982 Jan; 25(1):36-42. PMID: 6979298
Two cousins with trisomy for the distal third of 16q due to a familial translocation, t(16;21)(q22.2;q22-2), are reported. The APRT gene locus could be assigned to 16q22.2 to 16qter. The...
10.
Homocystinuria caused by 5,10-methylenetetrahydrofolate reductase deficiency: a case in an infant responding to methionine, folinic acid, pyridoxine, and vitamin B12 therapy
Harpey J, Rosenblatt D, Cooper B, Le Moel G, Roy C, LAFOURCADE J
J Pediatr . 1981 Feb; 98(2):275-8. PMID: 7007598
No abstract available.