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Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association
|
May 10, 2011
Long term clinical management of girls with Turner syndrome at a center of pediatric endocrinology
P Schonhoff, A Körner, J Kratzsch, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
January 1, 1993
[Glucose homeostasis in cystic fibrosis. Oral glucose tolerance test in comparison with formula administration]
H Skopnik, H Kentrup, G Kusenbach, et al.
European Journal of Endocrinology
|
September 1, 2005
A new heterozygous mutation of the FOXL2 gene is associated with a large ovarian cyst and ovarian dysfunction in an adolescent girl with blepharophimosis/ptosis/epicanthus inversus syndrome
K Raile, H Stobbe, R B Tröbs, et al.
Hormone Research
|
February 16, 2002
A new C-terminal located mutation (V272ter) in the PIT-1 gene manifesting with severe congenital hypothyroidism. Possible functionality of the PIT-1 C-terminus
O Blankenstein, R Mühlenberg, C Kim, et al.
Hormone Research
|
May 15, 2002
Familial combined pituitary hormone deficiency caused by PROP-1 gene mutation. Growth patterns and MRI studies in untreated subjects
J Crone, R Pfäffle, H Stobbe, et al.
AJNR. American Journal of Neuroradiology
|
June 28, 2000
Posterior pituitary ectopia: another hint toward a genetic etiology
D Maintz, G Benz-Bohm, A Gindele, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
September 1, 1995
Genetics and molecular biology in short stature
P E Mullis, J Argente, S Amselem, et al.
European Journal of Pediatrics
|
December 10, 1997
Combined pituitary deficiencies of growth hormone, thyroid stimulating hormone and prolactin due to Pit-1 gene mutation: a case report
R W Holl, R Pfäffle, C Kim, et al.
Hormone Research
|
January 1, 1996
Pit-1: clinical aspects
R Pfäffle, C Kim, B Otten, et al.
Klinische Padiatrie
|
December 1, 2007
[Results of an endocrinological follow-up of patients with childhood-or adolescent-onset malignancies]
A Keller, U Bierbach, J Mieke, et al.
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of 3
Search research articles
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Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association
|
May 10, 2011
Long term clinical management of girls with Turner syndrome at a center of pediatric endocrinology
P Schonhoff, A Körner, J Kratzsch, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
January 1, 1993
[Glucose homeostasis in cystic fibrosis. Oral glucose tolerance test in comparison with formula administration]
H Skopnik, H Kentrup, G Kusenbach, et al.
European Journal of Endocrinology
|
September 1, 2005
A new heterozygous mutation of the FOXL2 gene is associated with a large ovarian cyst and ovarian dysfunction in an adolescent girl with blepharophimosis/ptosis/epicanthus inversus syndrome
K Raile, H Stobbe, R B Tröbs, et al.
Hormone Research
|
February 16, 2002
A new C-terminal located mutation (V272ter) in the PIT-1 gene manifesting with severe congenital hypothyroidism. Possible functionality of the PIT-1 C-terminus
O Blankenstein, R Mühlenberg, C Kim, et al.
Hormone Research
|
May 15, 2002
Familial combined pituitary hormone deficiency caused by PROP-1 gene mutation. Growth patterns and MRI studies in untreated subjects
J Crone, R Pfäffle, H Stobbe, et al.
AJNR. American Journal of Neuroradiology
|
June 28, 2000
Posterior pituitary ectopia: another hint toward a genetic etiology
D Maintz, G Benz-Bohm, A Gindele, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
September 1, 1995
Genetics and molecular biology in short stature
P E Mullis, J Argente, S Amselem, et al.
European Journal of Pediatrics
|
December 10, 1997
Combined pituitary deficiencies of growth hormone, thyroid stimulating hormone and prolactin due to Pit-1 gene mutation: a case report
R W Holl, R Pfäffle, C Kim, et al.
Hormone Research
|
January 1, 1996
Pit-1: clinical aspects
R Pfäffle, C Kim, B Otten, et al.
Klinische Padiatrie
|
December 1, 2007
[Results of an endocrinological follow-up of patients with childhood-or adolescent-onset malignancies]
A Keller, U Bierbach, J Mieke, et al.
Page
of 3