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Applying the Schlossberg 4S Transition Model to Retired University Faculty: Does It Fit?
Published in:
Adultspan Journal, 2000, v. 2, n. 1, p. 15, doi. 10.1002/j.2161-0029.2000.tb00088.x
By:
- Goodman, Jane;
- Pappas, John G.
Publication type:
Article
Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype.
Published in:
American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 4, p. 822, doi. 10.1002/ajmg.a.35699
By:
- Burnside, Rachel D.;
- Pappas, John G.;
- Sacharow, Stephanie;
- Applegate, Carolyn;
- Hamosh, Ada;
- Gadi, Inder K.;
- Jaswaney, Vikram;
- Keitges, Elisabeth;
- Phillips, Karen K.;
- Potluri, Venketaswara R.;
- Risheg, Hiba;
- Smith, Janice L.;
- Tepperberg, Jim H.;
- Schwartz, Stuart;
- Papenhausen, Peter
Publication type:
Article
Client-perceptions of counselors-in-training: The effects of sex and gender role orientation.
Published in:
Counselor Education & Supervision, 1996, v. 35, n. 3, p. 190, doi. 10.1002/j.1556-6978.1996.tb00223.x
By:
- Ametrano, Irene Mass;
- Pappas, John G.
Publication type:
Article
Effect of Growth Hormone Therapy on Severe Short Stature and Skeletal Deformities in a Patient with Combined Turner Syndrome and Langer Mesomelic Dysplasia.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 12, p. 5028, doi. 10.1210/jc.2009-0679
By:
- Shah, Bina C.;
- Moran, Ellen S.;
- Zinn, Andrew R.;
- Pappas, John G.
Publication type:
Article
In vivo epigenetic editing of Sema6a promoter reverses transcallosal dysconnectivity caused by C11orf46/Arl14ep risk gene.
Published in:
Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12013-y
By:
- Peter, Cyril J.;
- Saito, Atsushi;
- Hasegawa, Yuto;
- Tanaka, Yuya;
- Nagpal, Mohika;
- Perez, Gabriel;
- Alway, Emily;
- Espeso-Gil, Sergio;
- Fayyad, Tariq;
- Ratner, Chana;
- Dincer, Aslihan;
- Gupta, Achla;
- Devi, Lakshmi;
- Pappas, John G.;
- Lalonde, François M.;
- Butman, John A.;
- Han, Joan C.;
- Akbarian, Schahram;
- Kamiya, Atsushi
Publication type:
Article
Unusual phenotype of congenital adrenal hyperplasia (CAH) with a novel mutation of the CYP21A2 gene.
Published in:
Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 867, doi. 10.1515/jpem-2015-0457
By:
- Raisingani, Manish;
- Contreras, Maria F.;
- Prasad, Kris;
- Pappas, John G.;
- Kluge, Michelle L.;
- Shah, Bina;
- David, Raphael
Publication type:
Article
PPP3CA truncating variants clustered in the regulatory domain cause early‐onset refractory epilepsy.
Published in:
Clinical Genetics, 2021, v. 100, n. 2, p. 227, doi. 10.1111/cge.13979
By:
- Panneerselvam, Sugi;
- Wang, Julia;
- Zhu, Wenmiao;
- Dai, Hongzheng;
- Pappas, John G.;
- Rabin, Rachel;
- Low, Karen J.;
- Rosenfeld, Jill A.;
- Emrick, Lisa;
- Xiao, Rui;
- Xia, Fan;
- Yang, Yaping;
- Eng, Christine M.;
- Anderson, Anne;
- Chau, Vann;
- Soler‐Alfonso, Claudia;
- Streff, Haley;
- Lalani, Seema R.;
- Mercimek‐Andrews, Saadet;
- Bi, Weimin
Publication type:
Article
Hyponatremic Seizures and Adrenal Hypoplasia Congenita in a Neonate with Congenital Diaphragmatic Hernia.
Published in:
Case Reports in Pediatrics, 2019, p. 1, doi. 10.1155/2019/4178251
By:
- Verma, Sourabh;
- Purrier, Sheryl;
- Breidbart, Emily;
- Pappas, John G.;
- Mally, Pradeep V.;
- Randis, Tara M.
Publication type:
Article
De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy.
Published in:
Annals of Clinical & Translational Neurology, 2015, v. 2, n. 6, p. 623, doi. 10.1002/acn3.198
By:
- Esmaeeli Nieh, Sahar;
- Madou, Maura R. Z.;
- Sirajuddin, Minhajuddin;
- Fregeau, Brieana;
- McKnight, Dianalee;
- Lexa, Katrina;
- Strober, Jonathan;
- Spaeth, Christine;
- Hallinan, Barbara E.;
- Smaoui, Nizar;
- Pappas, John G.;
- Burrow, Thomas A.;
- McDonald, Marie T.;
- Latibashvili, Mariam;
- Leshinsky ‐ Silver, Esther;
- Lev, Dorit;
- Blumkin, Luba;
- Vale, Ronald D.;
- Barkovich, Anthony James;
- Sherr, Elliott H.
Publication type:
Article

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