Search research articles
Contact Us
Filters
Showing results (1-10 of 12) with videos related to
Page
of 2
Sort By:
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
July 29, 2018
The effect of 17 years of increased salt iodization on the prevalence and nature of goiter in Croatian schoolchildren
Maja Vučinić, Vesna Kušec, Sandra Dundović, et al.
Collegium Antropologicum
|
January 30, 2004
Occlusal molar surfaces in females with Turner's syndrome
Mihajlo Maćesić, Zvonimir Kaić, Jelena Dumancić, et al.
American Journal of Medical Genetics
|
November 20, 2002
Choanal stenosis, hypothelia, deafness, recurrent dacryocystitis, neck fistulas, short stature, and microcephaly: report of a case
Miroslav Dumić, Marijana Cvitanović, Borna Sarić, et al.
Lijecnicki Vjesnik
|
June 15, 2010
[Low doses of sulphonyluria as a successful replacement for insulin therapy in a patient with neonatal diabetes due to a mutation of KCNJ11 gene encoding Kir6.2]
Jasenka Ille, Natasa Rojnić Putarek, Ana Radica, et al.
European Journal of Pediatrics
|
November 7, 2013
Primary hypothyroidism and nipple hypoplasia in a girl with Wolcott-Rallison syndrome
Anita Spehar Uroić, Vjosa Mulliqi Kotori, Nataša Rojnić Putarek, et al.
Lijecnicki Vjesnik
|
September 23, 2009
[Marden-Walker syndrome--a case report]
Miroslav Dumić, Natasa Rojnić-Putarek, Snjezana Skrablin-Kucić, et al.
European Journal of Pediatrics
|
October 9, 2010
Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy
Miroslav Dumić, Nina Barišić, Nataša Rojnić-Putarek, et al.
Archives of Oral Biology
|
July 4, 2016
Growth hormone positive effects on craniofacial complex in Turner syndrome
Jovana Juloski, Jelena Dumančić, Ivana Šćepan, et al.
Lijecnicki Vjesnik
|
August 19, 2007
[Three-year-old boy--a homozygote for familiar hypercholesterolemia]
Miroslav Dumić, Anita Spehar Uroic, Igor Francetić, et al.
Lijecnicki Vjesnik
|
November 30, 2006
[Primary pigmented nodular adrenocortical disease as cause of Cushing's syndrome associated with Carney complex]
Miroslav Dumić, Nevena Janjanin, Anita Spehar Uroić, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
July 29, 2018
The effect of 17 years of increased salt iodization on the prevalence and nature of goiter in Croatian schoolchildren
Maja Vučinić, Vesna Kušec, Sandra Dundović, et al.
Collegium Antropologicum
|
January 30, 2004
Occlusal molar surfaces in females with Turner's syndrome
Mihajlo Maćesić, Zvonimir Kaić, Jelena Dumancić, et al.
American Journal of Medical Genetics
|
November 20, 2002
Choanal stenosis, hypothelia, deafness, recurrent dacryocystitis, neck fistulas, short stature, and microcephaly: report of a case
Miroslav Dumić, Marijana Cvitanović, Borna Sarić, et al.
Lijecnicki Vjesnik
|
June 15, 2010
[Low doses of sulphonyluria as a successful replacement for insulin therapy in a patient with neonatal diabetes due to a mutation of KCNJ11 gene encoding Kir6.2]
Jasenka Ille, Natasa Rojnić Putarek, Ana Radica, et al.
European Journal of Pediatrics
|
November 7, 2013
Primary hypothyroidism and nipple hypoplasia in a girl with Wolcott-Rallison syndrome
Anita Spehar Uroić, Vjosa Mulliqi Kotori, Nataša Rojnić Putarek, et al.
Lijecnicki Vjesnik
|
September 23, 2009
[Marden-Walker syndrome--a case report]
Miroslav Dumić, Natasa Rojnić-Putarek, Snjezana Skrablin-Kucić, et al.
European Journal of Pediatrics
|
October 9, 2010
Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy
Miroslav Dumić, Nina Barišić, Nataša Rojnić-Putarek, et al.
Archives of Oral Biology
|
July 4, 2016
Growth hormone positive effects on craniofacial complex in Turner syndrome
Jovana Juloski, Jelena Dumančić, Ivana Šćepan, et al.
Lijecnicki Vjesnik
|
August 19, 2007
[Three-year-old boy--a homozygote for familiar hypercholesterolemia]
Miroslav Dumić, Anita Spehar Uroic, Igor Francetić, et al.
Lijecnicki Vjesnik
|
November 30, 2006
[Primary pigmented nodular adrenocortical disease as cause of Cushing's syndrome associated with Carney complex]
Miroslav Dumić, Nevena Janjanin, Anita Spehar Uroić, et al.
Page
of 2