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Items: 7

1.

Using the PHQ-9 and GAD-7 to screen for acute distress in transgender youth: findings from a pediatric endocrinology clinic.

Moyer DN, Connelly KJ, Holley AL.

J Pediatr Endocrinol Metab. 2019 Jan 28;32(1):71-74. doi: 10.1515/jpem-2018-0408.

PMID:
30530884
2.

A degradation fragment of type X collagen is a real-time marker for bone growth velocity.

Coghlan RF, Oberdorf JA, Sienko S, Aiona MD, Boston BA, Connelly KJ, Bahney C, LaRouche J, Almubarak SM, Coleman DT, Girkontaite I, von der Mark K, Lunstrum GP, Horton WA.

Sci Transl Med. 2017 Dec 6;9(419). pii: eaan4669. doi: 10.1126/scitranslmed.aan4669.

3.

Detecting Congenital Central Hypothyroidism by Newborn Screening: Difficulty in Distinguishing from Congenital Thyroxine-Binding Globulin Deficiency.

Connelly KJ, Pierce MJ, Hanna C, LaFranchi SH.

Horm Res Paediatr. 2017;88(5):331-338. doi: 10.1159/000479367. Epub 2017 Sep 14.

PMID:
28910808
4.

Thrombotic issues in transgender medicine: A review.

Shatzel JJ, Connelly KJ, DeLoughery TG.

Am J Hematol. 2017 Feb;92(2):204-208. doi: 10.1002/ajh.24593. Review.

5.

Neonatal estrogen exposure results in biphasic age-dependent effects on the skeletal development of male mice.

Connelly KJ, Larson EA, Marks DL, Klein RF.

Endocrinology. 2015 Jan;156(1):193-202. doi: 10.1210/en.2014-1324.

6.

Detection of neonates with mild congenital hypothyroidism (primary) or isolated hyperthyrotropinemia: an increasingly common management dilemma.

Connelly KJ, LaFranchi SH.

Expert Rev Endocrinol Metab. 2014 May;9(3):263-271. doi: 10.1586/17446651.2014.897607. Epub 2014 Mar 17.

PMID:
30736165
7.

Congenital hypothyroidism caused by excess prenatal maternal iodine ingestion.

Connelly KJ, Boston BA, Pearce EN, Sesser D, Snyder D, Braverman LE, Pino S, LaFranchi SH.

J Pediatr. 2012 Oct;161(4):760-2. doi: 10.1016/j.jpeds.2012.05.057. Epub 2012 Jul 27.

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