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Journal of Endocrinological Investigation
|
May 14, 2008
In the Italian population sexual dimorphism affects pre-natal thyroid migration but not biochemical severity of gland ectopia and pre-natal bone maturation
M Wasniewska, T Arrigo, G Crisafulli, et al.
Journal of Endocrinological Investigation
|
November 11, 2008
Combined treatment with ketoconazole and cyproterone acetate in a boy with McCune-Albright syndrome and peripheral precocious puberty
M F Messina, T Arrigo, M Wasniewska, et al.
Diabetes, Nutrition & Metabolism
|
November 6, 2002
Two-year prospective evaluation of the factors affecting honeymoon frequency and duration in children with insulin dependent diabetes mellitus: the key-role of age at diagnosis
F Lombardo, M Valenzise, M Wasniewska, et al.
Journal of Endocrinological Investigation
|
February 18, 2006
Salt wasting phenotype in a compound heterozygous girl with P482S mutation associated with anovel mutation of CYP21 gene (Q481P)
G Di Pasquale, M Wasniewska, M Caruso, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 16, 1998
[Hypopituitarism during the first year of life. A collaborative Italian study]
De Luca Ff2p4, T Arrigo, M Bozzola, et al.
Biochemical and Biophysical Research Communications
|
May 9, 2001
Abnormal calcium homeostasis in fibroblasts from patients with Leigh disease
M Wasniewska, E Karczmarewicz, M Pronicki, et al.
Journal of Endocrinological Investigation
|
July 29, 2009
Severe SHOX gene haploinsufficiency in a girl with a novel mutation (M1T) involving the first codon of coding region
M Wasniewska, G Raiola, A Nicoletti, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
November 20, 2013
[A not very essential obesity: the Rohhad syndrome. Description of two cases and review of the literature]
V Ramistella, M Wasniewska, M Valenzise, et al.
Journal of Endocrinological Investigation
|
April 20, 2011
Early hypertension and prolonged mineralocorticoid therapy discontinuation in a child with salt-wasting 21-hydroxylase deficiency
M Wasniewska, M Valenzise, T Aversa, et al.
Journal of Endocrinological Investigation
|
September 13, 2008
Salt-wasting congenital adrenal hyperplasia: genotypical peculiarities in a Sicilian ethnic group
M Wasniewska, M Caruso, S Indovina, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 67) with videos related to
Sort By:
Page
of 7
Journal of Endocrinological Investigation
|
May 14, 2008
In the Italian population sexual dimorphism affects pre-natal thyroid migration but not biochemical severity of gland ectopia and pre-natal bone maturation
M Wasniewska, T Arrigo, G Crisafulli, et al.
Journal of Endocrinological Investigation
|
November 11, 2008
Combined treatment with ketoconazole and cyproterone acetate in a boy with McCune-Albright syndrome and peripheral precocious puberty
M F Messina, T Arrigo, M Wasniewska, et al.
Diabetes, Nutrition & Metabolism
|
November 6, 2002
Two-year prospective evaluation of the factors affecting honeymoon frequency and duration in children with insulin dependent diabetes mellitus: the key-role of age at diagnosis
F Lombardo, M Valenzise, M Wasniewska, et al.
Journal of Endocrinological Investigation
|
February 18, 2006
Salt wasting phenotype in a compound heterozygous girl with P482S mutation associated with anovel mutation of CYP21 gene (Q481P)
G Di Pasquale, M Wasniewska, M Caruso, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 16, 1998
[Hypopituitarism during the first year of life. A collaborative Italian study]
De Luca Ff2p4, T Arrigo, M Bozzola, et al.
Biochemical and Biophysical Research Communications
|
May 9, 2001
Abnormal calcium homeostasis in fibroblasts from patients with Leigh disease
M Wasniewska, E Karczmarewicz, M Pronicki, et al.
Journal of Endocrinological Investigation
|
July 29, 2009
Severe SHOX gene haploinsufficiency in a girl with a novel mutation (M1T) involving the first codon of coding region
M Wasniewska, G Raiola, A Nicoletti, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
November 20, 2013
[A not very essential obesity: the Rohhad syndrome. Description of two cases and review of the literature]
V Ramistella, M Wasniewska, M Valenzise, et al.
Journal of Endocrinological Investigation
|
April 20, 2011
Early hypertension and prolonged mineralocorticoid therapy discontinuation in a child with salt-wasting 21-hydroxylase deficiency
M Wasniewska, M Valenzise, T Aversa, et al.
Journal of Endocrinological Investigation
|
September 13, 2008
Salt-wasting congenital adrenal hyperplasia: genotypical peculiarities in a Sicilian ethnic group
M Wasniewska, M Caruso, S Indovina, et al.
Page
of 7