Weill J - Search Results

1

Congenital disorder of glycosylation Ib (CDG-Ib) without gastrointestinal symptoms.

Penel-Capelle D, Dobbelaere D, Jaeken J, Klein A, Cartigny M, Weill J. Penel-Capelle D, et al. Among authors: weill j. J Inherit Metab Dis. 2003;26(1):83-5. doi: 10.1023/a:1024044017385. J Inherit Metab Dis. 2003. PMID: 12872847

2

[Type Ib pseudohypoaldosteronism: clinical aspects and nosological problems. Apropos of 3 cases].

Espinasse-Holder M, Vanderbecken S, Cartigny M, Stuckens C, Weill J. Espinasse-Holder M, et al. Among authors: weill j. Arch Pediatr. 1999 Oct;6(10):1077-80. doi: 10.1016/s0929-693x(00)86983-3. Arch Pediatr. 1999. PMID: 10544784 French.

3

[Regional network for neonatal screening and management of affected patients].

Farriaux JP, Turck D, Sardet A, Weill J, Dobbelaere D, Cartigny M, Lambilliotte A. Farriaux JP, et al. Among authors: weill j. Arch Pediatr. 2003 May;10 Suppl 1:24s-27s. doi: 10.1016/s0929-693x(03)90369-1. Arch Pediatr. 2003. PMID: 14509729 French. No abstract available.

4

Childhood-onset narcolepsy, obesity and puberty in four consecutive children: a close temporal link.

Perriol MP, Cartigny M, Lamblin MD, Poirot I, Weill J, Derambure P, Monaca C. Perriol MP, et al. Among authors: weill j. J Pediatr Endocrinol Metab. 2010 Mar;23(3):257-65. doi: 10.1515/jpem.2010.23.3.257. J Pediatr Endocrinol Metab. 2010. PMID: 20480724

5

Congenital diserythropoietic anemia type I. Report on monozygotic twins with associated hemochromatosis and short stature.

Facon T, Mannessier L, Lepelley P, Weill J, Fenaux P, Dupriez B, Morel P, Jouet JP. Facon T, et al. Among authors: weill j. Blut. 1990 Oct;61(4):248-50. doi: 10.1007/BF01744140. Blut. 1990. PMID: 2224147

6

Understanding the rising incidence of type 2 diabetes in adolescence.

Weill J, Vanderbecken S, Froguel P. Weill J, et al. Arch Dis Child. 2004 Jun;89(6):502-4. doi: 10.1136/adc.2003.028548. Arch Dis Child. 2004. PMID: 15155389 Free PMC article. No abstract available.

7

[Neonatal screening of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Lille experience 1980-1996].

Cartigny-Maciejewski M, Guilley N, Vanderbecken S, Gondé S, Stuckens C, Ponté C, Weill J, Farriaux JP, Paux E. Cartigny-Maciejewski M, et al. Among authors: weill j. Arch Pediatr. 1999 Feb;6(2):151-8. doi: 10.1016/s0929-693x(99)80202-4. Arch Pediatr. 1999. PMID: 10079883 French.

8

[Medical strategy: growth hormone, indications, modalities and results].

Weill J, Vanuxeem C. Weill J, et al. Soins Pediatr Pueric. 2000 Mar-Apr;(193):26-8. Soins Pediatr Pueric. 2000. PMID: 11040796 French. No abstract available.

9

[Transient complete somatotropin insufficiency. A retrospective study].

Weill J, Stuckens C, Ponte C. Weill J, et al. Pediatrie. 1990;45(5):327-32. Pediatrie. 1990. PMID: 2165246 French.

10

[Ichthyosis linked to the X chromosome. Biochemical and endocrinologic study].

Weill J, Vasseur F, Savary JB, Stuckens C, Deminatti MM, Ponte C. Weill J, et al. Pediatrie. 1989;44(7):559-62. Pediatrie. 1989. PMID: 2530495 French.

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