Filter

Refine by collections

  • Bone and Mineral Metabolism (3)

Refine by date

—
  • Print
  • Save

Search Results

You are looking at 1 - 3 of 3 items for :

  • "congenital" x
  • Bone and Mineral Metabolism x
Clear All
Anna Liori Division of Endocrinology, Department of Internal Medicine, University of Patras, School of Health Sciences, Patras, Greece

Search for other papers by Anna Liori in
Google Scholar
PubMed Close
,
Damaskini Polychroni Division of Endocrinology, Department of Internal Medicine, University of Patras, School of Health Sciences, Patras, Greece

Search for other papers by Damaskini Polychroni in
Google Scholar
PubMed Close
,
Georgios K Markantes Division of Endocrinology, Department of Internal Medicine, University of Patras, School of Health Sciences, Patras, Greece

Search for other papers by Georgios K Markantes in
Google Scholar
PubMed Close
,
Maria Stamou Division of Endocrinology, Department of Internal Medicine, University of Patras, School of Health Sciences, Patras, Greece

Search for other papers by Maria Stamou in
Google Scholar
PubMed Close
,
Sarantis Livadas Endocrine Unit, Athens Medical Centre, Athens, Greece

Search for other papers by Sarantis Livadas in
Google Scholar
PubMed Close
,
George Mastorakos Unit of Endocrinology, Diabetes Mellitus and Metabolism, Aretaieion Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece

Search for other papers by George Mastorakos in
Google Scholar
PubMed Close
, and
Neoklis Georgopoulos Division of Endocrinology, Department of Internal Medicine, University of Patras, School of Health Sciences, Patras, Greece

Search for other papers by Neoklis Georgopoulos in
Google Scholar
PubMed Close

, 21 ), lower birth weight for their offspring ( 22 ), preterm deliveries ( 23 ) and neonatal congenital abnormalities ( 23 ) than women from their host countries. Endocrinopathies are common diseases among women of reproductive age, and thus

Article Type:
Research Article
Collections:
Bone and Mineral Metabolism
DOI:
https://doi.org/10.1530/EC-21-0412
Volume/Issue:
Volume 11: Issue 1
Open access
Róża Aleksandrowicz Department of Prophylaxis of Metabolic Diseases, Bialystok, Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, Poland

Search for other papers by Róża Aleksandrowicz in
Google Scholar
PubMed Close
and
Marek Strączkowski Department of Prophylaxis of Metabolic Diseases, Bialystok, Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, Poland

Search for other papers by Marek Strączkowski in
Google Scholar
PubMed Close

congenital muscular dystrophy . Cells 2019 8 459. ( https://doi.org/10.3390/cells8050459 ) 19 Guiraud S Migeon T Ferry A Chen Z Ouchelouche S Verpont MC Sado Y Allamand V Ronco P Plaisier E , HANAC Col4a1 mutation in mice leads to

Article Type:
Review Article
Collections:
Bone and Mineral Metabolism
DOI:
https://doi.org/10.1530/EC-23-0023
Volume/Issue:
Volume 12: Issue 5
Open access
Lu Yang Department of Nuclear Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China

Search for other papers by Lu Yang in
Google Scholar
PubMed Close
,
Xingguo Jing Department of Nuclear Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China

Search for other papers by Xingguo Jing in
Google Scholar
PubMed Close
,
Hua Pang Department of Nuclear Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China

Search for other papers by Hua Pang in
Google Scholar
PubMed Close
,
Lili Guan Department of Nuclear Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China

Search for other papers by Lili Guan in
Google Scholar
PubMed Close
, and
Mengdan Li Department of Nuclear Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China

Search for other papers by Mengdan Li in
Google Scholar
PubMed Close

of histological cellular hyperplasia in more than one gland after surgical and pathological evaluation of any enlarged gland ( 17 ). Sporadic MGD, on the other hand, is described on the basis of the exclusion of congenital and familial PHPT. Regarding

Article Type:
Review Article
Collections:
Bone and Mineral Metabolism
DOI:
https://doi.org/10.1530/EC-23-0492
Volume/Issue:
Volume 13: Issue 5
Open access