Muge Calikoglu: search on Z-Library

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1

Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations

Chinsky, Jeffrey M, Singh, Rani, Ficicioglu, Can, van Karnebeek, Clara D M, Grompe, Markus, Mitchell, Grant, Waisbren, Susan E, Gucsavas-Calikoglu, Muge, Wasserstein, Melissa P, Coakley, Katie, Scott,

Journal:

Genetics in Medicine

Year:

2017

Language:

english

File:

PDF, 392 KB

english, 2017

2

A clinical report of a patient with two abnormal cell lines: 46,XX,del(21)(q22.1) and 47,XX,+3

Denise I. Quigley, Jeffery Sailus, Kathleen Kaiser-Rogers, Kathleen W. Rao, Muge Calikoglu, Stuart Gold, Shawn E. McCandless

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 105 KB

english, 2005

3

Expanding spectrum of congenital disorder of glycosylation Ig (CDG-Ig): Sibs with a unique skeletal dysplasia, hypogammaglobulinemia, cardiomyopathy, genital malformations, and early lethality

Christian Kranz, Alice A. Basinger, Müge Güçsavaş-Çalıkoğlu, Liangwu Sun, Cynthia M. Powell, Frederick W. Henderson, Arthur S. Aylsworth, Hudson H. Freeze

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 308 KB

english, 2007

4

A phase I/II clinical trial of enzyme replacement therapy in mucopolysaccharidosis II (Hunter syndrome)

Joseph Muenzer, Muge Gucsavas-Calikoglu, Shawn E. McCandless, Thomas J. Schuetz, Alan Kimura

Journal:

Molecular Genetics and Metabolism

Year:

2007

Language:

english

File:

PDF, 300 KB

english, 2007

5

A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome)

Muenzer, Joseph, Wraith, James E, Beck, Michael, Giugliani, Roberto, Harmatz, Paul, Eng, Christine M, Vellodi, Ashok, Martin, Rick, Ramaswami, Uma, Gucsavas-Calikoglu, Muge, Vijayaraghavan, Suresh, We

Journal:

Genetics in Medicine

Year:

2006

Language:

english

File:

PDF, 454 KB

english, 2006

6

Long-term, open-labeled extension study of idursulfase in the treatment of Hunter syndrome

Muenzer, Joseph, Beck, Michael, Eng, Christine M, Giugliani, Roberto, Harmatz, Paul, Martin, Rick, Ramaswami, Uma, Vellodi, Ashok, Wraith, James E, Cleary, Maureen, Gucsavas-Calikoglu, Muge, Puga, Ana

Journal:

Genetics in Medicine

Year:

2011

Language:

english

File:

PDF, 498 KB

english, 2011

7

CORRIGENDUM: Long-term, open-labeled extension study of idursulfase in the treatment of Hunter syndrome

Muenzer, Joseph, Beck, Michael, Eng, Christine M, Giugliani, Roberto, Harmatz, Paul, Martin, Rick, Ramaswami, Uma, Vellodi, Ashok, Wraith, James E, Cleary, Maureen, Gucsavas-Calikoglu, Muge, Puga, Ana

Journal:

Genetics in Medicine

Year:

2013

Language:

english

File:

PDF, 80 KB

english, 2013

8

Co-occurring Down syndrome and SUCLA2 -related mitochondrial depletion syndrome

Couser, Natario L., Marchuk, Daniel S., Smith, Laurie D., Arreola, Alexandra, Kaiser-Rogers, Kathleen A., Muenzer, Joseph, Pandya, Arti, Gucsavas-Calikoglu, Muge, Powell, Cynthia M.

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 563 KB

english, 2017

9

Trampoline-related Injuries to Children

Hartmann, Katherine E., Çalikoglu, Müge G.

Journal:

Year:

1999

Language:

english

File:

PDF, 389 KB

english, 1999