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Annales De Chirurgie Infantile
|
September 1, 1972
[2 cases of virilizing adrenal cortex tumors in infants]
J Prevot, M Mourot, G Lascombes, et al.
Archives Francaises De Pediatrie
|
May 1, 1980
[Neonatal hyperparathyroidism secondary to maternal hypoparathyroidism (author's transl)]
M Vidailhet, P Monin, M André, et al.
Archives Francaises De Pediatrie
|
April 1, 1982
[Benign pheochromocytoma and metaphyseal bone lesions in childhood]
C Delgoffe, M C Bretagne, J C Hoeffel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 1, 1995
"Pure" striatonigral degeneration and Parkinson's disease: a comparative clinical study
N Gouider-Khouja, M Vidailhet, A M Bonnet, et al.
Human Genetics
|
January 19, 1979
Isoelectrofocusing of erythrocyte galactose 1 phospho uridyl transferase in a family with both galactosemia and Duarte variants
F Schapira, C Gregori, J Banroques, et al.
European Journal of Neurology
|
February 13, 2013
PRRT2 mutations and paroxysmal disorders
A Méneret, C Gaudebout, F Riant, et al.
La Revue De Medecine Interne
|
January 1, 1992
[Involvement of central nervous system disclosing Waldenstrom's disease: demonstration of intrathecal secretion of immunoglobulin M]
O Fain, B Wechsler, M Vidailhet, et al.
Australasian Radiology
|
March 1, 1976
Malformations of the hand associated with congenital heart lesions
J C Hoeffel, C Pernot, A M Worms, et al.
Archives Francaises De Pediatrie
|
May 1, 1970
[Partial and transitory erythrocyte galactokinase deficiency in a newborn. Biochemical study]
C Vigneron, C Marchal, C Deifts, et al.
Archives Francaises De Pediatrie
|
November 1, 1970
[Metachromatic leucodystrophy or sulfatidosis in children]
C Marchal, M Vidailhet, C Vidailhet, et al.
Page
of 31
Search research articles
Search
Showing results (111-120 of 303) with videos related to
Sort By:
Page
of 31
Annales De Chirurgie Infantile
|
September 1, 1972
[2 cases of virilizing adrenal cortex tumors in infants]
J Prevot, M Mourot, G Lascombes, et al.
Archives Francaises De Pediatrie
|
May 1, 1980
[Neonatal hyperparathyroidism secondary to maternal hypoparathyroidism (author's transl)]
M Vidailhet, P Monin, M André, et al.
Archives Francaises De Pediatrie
|
April 1, 1982
[Benign pheochromocytoma and metaphyseal bone lesions in childhood]
C Delgoffe, M C Bretagne, J C Hoeffel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 1, 1995
"Pure" striatonigral degeneration and Parkinson's disease: a comparative clinical study
N Gouider-Khouja, M Vidailhet, A M Bonnet, et al.
Human Genetics
|
January 19, 1979
Isoelectrofocusing of erythrocyte galactose 1 phospho uridyl transferase in a family with both galactosemia and Duarte variants
F Schapira, C Gregori, J Banroques, et al.
European Journal of Neurology
|
February 13, 2013
PRRT2 mutations and paroxysmal disorders
A Méneret, C Gaudebout, F Riant, et al.
La Revue De Medecine Interne
|
January 1, 1992
[Involvement of central nervous system disclosing Waldenstrom's disease: demonstration of intrathecal secretion of immunoglobulin M]
O Fain, B Wechsler, M Vidailhet, et al.
Australasian Radiology
|
March 1, 1976
Malformations of the hand associated with congenital heart lesions
J C Hoeffel, C Pernot, A M Worms, et al.
Archives Francaises De Pediatrie
|
May 1, 1970
[Partial and transitory erythrocyte galactokinase deficiency in a newborn. Biochemical study]
C Vigneron, C Marchal, C Deifts, et al.
Archives Francaises De Pediatrie
|
November 1, 1970
[Metachromatic leucodystrophy or sulfatidosis in children]
C Marchal, M Vidailhet, C Vidailhet, et al.
Page
of 31