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1.
The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency.
J Clin Endocrinol Metab
; 83(9): 3346-9, 1998 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-9745452
2.
Antibodies to pituitary surface antigens during various pituitary disease states.
J Endocrinol
; 175(2): 417-23, 2002 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-12429039
3.
Rarity of PIT1 involvement in children from Russia with combined pituitary hormone deficiency.
Am J Med Genet
; 77(5): 360-5, 1998 Jun 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-9632165
4.
Gene analysis of PROP1 in dwarfism with combined pituitary hormone deficiency.
Growth Horm IGF Res
; 9 Suppl B: 12-7, 1999 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-10549300
5.
[Study of the effectiveness and safety of Rastan in children with growth hormone deficiency and Turner's syndrome].
Probl Endokrinol (Mosk)
; 53(2): 40-44, 2007 Apr 15.
Artículo
en Ruso
| MEDLINE | ID: mdl-31627576
6.
GH-1 gene splicing mutations: molecular basis of hereditary isolated growth hormone deficiency in children.
Bull Exp Biol Med
; 141(3): 347-52, 2006 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-17073157
7.
[Effectiveness and safety of replacement treatment with the growth hormone drug Saizen in a new formulation].
Probl Endokrinol (Mosk)
; 52(4): 28-31, 2006 Aug 15.
Artículo
en Ruso
| MEDLINE | ID: mdl-31627640
8.
[The effectiveness and safety of use of a soluble recombinant growth hormone formulation in the treatment of shortness in children with retarded intrauterine development].
Probl Endokrinol (Mosk)
; 51(4): 26-31, 2005 Aug 15.
Artículo
en Ruso
| MEDLINE | ID: mdl-31627546
9.
[Clinical assessment of the role of circadian rhythm of hormone contents in the blood and saliva of children with congenital dysfunction of the adrenal cortex]. / Klinicheskaia otsenka roli sutochnykh ritmov soderzhaniia gormonov v krovi i sliune u detei s vrozhdennoi disfunktsiei kory nadpochechnikov.
Pediatriia
; (11): 38-41, 1989.
Artículo
en Ruso
| MEDLINE | ID: mdl-2608371
10.
[Methodical approaches to the determination of steroid hormone levels in different biological fluids in children with congenital dysfunction of the adrenal cortex]. / Metodicheskie podkhody k opredeleniu urovnei steroidnykh gormonov v razlichnykh biologicheskikh zhidkostiakh pri vrozhdennoi disfunktsii kory nadpochechnikov u detei.
Pediatriia
; (11): 72-5, 1989.
Artículo
en Ruso
| MEDLINE | ID: mdl-2608377
11.
[Attempt to use the genetically engineered growth hormone SAIZEN in children with somatotropic insufficiency: results of clinical trials in Russia]. / Opyt ispol'zovaniia genno-inzhenernogo gormona rosta SAIZEN dlia lecheniia detei s somatotropnoi nedostatochnost'iu: rezul'taty klinicheskoi aprobatsii v Rossii.
Probl Endokrinol (Mosk)
; 40(6): 30-4, 1994.
Artículo
en Ruso
| MEDLINE | ID: mdl-7740034
12.
A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasia.
Endocr J
; 45(6): 791-5, 1998 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-10395236
13.
A mutational hot spot in the Prop-1 gene in Russian children with combined pituitary hormone deficiency.
Pituitary
; 1(1): 45-9, 1998 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-11081182
14.
[Case of severe insulin-resistant diabetes mellitus in a 2-year-old girl]. / Sluchai tiazhelogo insulinrezistentnogo sakharnogo diabeta u devochki 2-letnego vozrasta.
Pediatriia
; (4): 79-81, 1987.
Artículo
en Ruso
| MEDLINE | ID: mdl-3601566
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