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Literature DB >> 19321197

Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients.

Laura Tassone, Lucia D Notarangelo, Vanessa Bonomi, Gianfranco Savoldi, Alberto Sensi, Annarosa Soresina, C I Edvard Smith, Fulvio Porta, Alessandro Plebani, Luigi D Notarangelo, Raffaele Badolato.

Abstract

Entities: Disease Species

Mesh：

Substances：

Year: 2009 PMID： 19321197 DOI： 10.1016/j.jaci.2008.12.1133

Source DB: PubMed Journal: J Allergy Clin Immunol ISSN： 0091-6749 Impact factor: 10.793

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15 in total

1. Chromothriptic cure of WHIM syndrome.

Authors: David H McDermott; Ji-Liang Gao; Qian Liu; Marie Siwicki; Craig Martens; Paejonette Jacobs; Daniel Velez; Erin Yim; Christine R Bryke; Nancy Hsu; Zunyan Dai; Martha M Marquesen; Elina Stregevsky; Nana Kwatemaa; Narda Theobald; Debra A Long Priel; Stefania Pittaluga; Mark A Raffeld; Katherine R Calvo; Irina Maric; Ronan Desmond; Kevin L Holmes; Douglas B Kuhns; Karl Balabanian; Françoise Bachelerie; Stephen F Porcella; Harry L Malech; Philip M Murphy
Journal: Cell Date: 2015-02-05 Impact factor: 41.582

2. Plerixafor for the Treatment of WHIM Syndrome.

Authors: David H McDermott; Diana V Pastrana; Katherine R Calvo; Stefania Pittaluga; Daniel Velez; Elena Cho; Qian Liu; Hugh H Trout; João F Neves; Pamela J Gardner; David A Bianchi; Elizabeth A Blair; Emily M Landon; Susana L Silva; Christopher B Buck; Philip M Murphy
Journal: N Engl J Med Date: 2019-01-10 Impact factor: 91.245

Review 3. Genetics on a WHIM.

Authors: Omar Al Ustwani; Razelle Kurzrock; Meir Wetzler
Journal: Br J Haematol Date: 2013-09-20 Impact factor: 6.998

Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients.

1. Chromothriptic cure of WHIM syndrome.

2. Plerixafor for the Treatment of WHIM Syndrome.

Review 3. Genetics on a WHIM.

Review 4. Multisystem multitasking by CXCL12 and its receptors CXCR4 and ACKR3.

Review 5. Advances in basic and clinical immunology in 2009.

6. Oligoclonality, impaired class switch and B-cell memory responses in WHIM syndrome.

Review 7. Congenital neutropenia: diagnosis, molecular bases and patient management.

Review 8. WHIM Syndrome: from Pathogenesis Towards Personalized Medicine and Cure.

9. Pathogenesis, diagnosis and therapeutic strategies in WHIM syndrome immunodeficiency.

10. Hierarchical organization of multi-site phosphorylation at the CXCR4 C terminus.