Works matching Hermansky-Pudlak syndrome

Results: 388

Hermansky-Pudlak syndrome: Report of two patients with updated genetic classification and management recommendations.

Published in:

Pediatric Dermatology, 2017, v. 34, n. 6, p. 638, doi. 10.1111/pde.13266

By:

Loredana Asztalos, Manuela;
Schafernak, Kristian T.;
Gray, Jayla;
Berry, Adam;
Paller, Amy S.;
Mancini, Anthony J.

Publication type:

Article

Clinico-molecular analysis of eleven patients with Hermansky-Pudlak type 5 syndrome, a mild form of HPS.

Published in:

Pigment Cell & Melanoma Research, 2017, v. 30, n. 6, p. 563, doi. 10.1111/pcmr.12608

By:

Michaud, Vincent;
Lasseaux, Eulalie;
Plaisant, Claudio;
Verloes, Alain;
Perdomo ‐ Trujillo, Yaumara;
Hamel, Christian;
Elcioglu, Nursel H.;
Leroy, Bart;
Kaplan, Josseline;
Jouk, Pierre ‐ Simon;
Lacombe, Didier;
Fergelot, Patricia;
Morice ‐ Picard, Fanny;
Arveiler, Benoit

Publication type:

Article

NGS-based 100-gene panel of hypopigmentation identifies mutations in Chinese Hermansky-Pudlak syndrome patients.

Published in:

Pigment Cell & Melanoma Research, 2016, v. 29, n. 6, p. 702, doi. 10.1111/pcmr.12534

By:

Wei, Aihua;
Yuan, Yefeng;
Bai, Dayong;
Ma, Jing;
Hao, Zhenhua;
Zhang, Yingzi;
Yu, Jiaying;
Zhou, Zhiyong;
Yang, Lin;
Yang, Xiumin;
Li, Li;
Li, Wei

Publication type:

Article

Hermansky- Pudlak syndrome: pigmentary and non-pigmentary defects and their pathogenesis.

Published in:

Pigment Cell & Melanoma Research, 2013, v. 26, n. 2, p. 176, doi. 10.1111/pcmr.12051

By:

Wei, Ai‐Hua;
Li, Wei

Publication type:

Article

Natural killer cell activity and dysfunction in Hermansky-Pudlak syndrome.

Published in:

British Journal of Haematology, 2017, v. 176, n. 1, p. 118, doi. 10.1111/bjh.14390

By:

Gil‐Krzewska, Aleksandra;
Murakami, Yousuke;
Peruzzi, Giovanna;
O'Brien, Kevin J.;
Merideth, Melissa A.;
Cullinane, Andrew R.;
Gahl, William A.;
Coligan, John E.;
Gochuico, Bernadette R.;
Krzewski, Konrad

Publication type:

Article

Infantile-onset inflammatory bowel disease in a patient with Hermansky-Pudlak syndrome: a case report.

Published in:

2019

By:

Ishihara, Jun;
Mizuochi, Tatsuki;
Uchida, Takashi;
Takaki, Yugo;
Konishi, Ken-ichiro;
Joo, Masahiko;
Takahashi, Yasuhiko;
Yoshioka, Shinichiro;
Kusano, Hironori;
Sasahara, Yoji;
Yamashita, Yushiro

Publication type:

journal article

Acute exacerbation of combined pulmonary fibrosis and emphysema associated with Hermansky- Pudlak syndrome.

Published in:

Respirology Case Reports, 2016, v. 4, n. 1, p. 13, doi. 10.1002/rcr2.141

By:

Sugino, Keishi;
Gocho, Kyoko;
Kikuchi, Naoshi;
Shibuya, Kazutoshi;
Uekusa, Toshimasa;
Homma, Sakae

Publication type:

Article

Instability of BLOC‐2 and BLOC‐3 in Chinese patients with Hermansky‐Pudlak syndrome.

Published in:

Pigment Cell & Melanoma Research, 2019, v. 32, n. 3, p. 373, doi. 10.1111/pcmr.12748

By:

Wei, Aihua;
Yuan, Yefeng;
Qi, Zhan;
Liu, Teng;
Bai, Dayong;
Zhang, Yingzi;
Yu, Jiaying;
Yang, Lin;
Yang, Xiumin;
Li, Wei

Publication type:

Article

A BLOC-1 mutation screen reveals a novel BLOC1S3 mutation in Hermansky-Pudlak Syndrome type 8.

Published in:

Pigment Cell & Melanoma Research, 2012, v. 25, n. 5, p. 584, doi. 10.1111/j.1755-148X.2012.01029.x

By:

Cullinane, Andrew R.;
Curry, James A.;
Golas, Gretchen;
Pan, James;
Carmona-Rivera, Carmelo;
Hess, Richard A.;
White, James G.;
Huizing, Marjan;
Gahl, William A.

Publication type:

Article

Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2.

Published in:

BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-42

By:

Jones, Matthew L.;
Murden, Sherina L.;
Brooks, Claire;
Maloney, Viv;
Manning, Richard A.;
Gilmour, Kimberly C.;
Bharadwaj, Vandana;
de la Fuente, Josu;
Chakravorty, Subarna;
Mumford, Andrew D.

Publication type:

Article

Hermansky-Pudlak syndrome and oculocutaneous albinism in Chinese children with pigmentation defects and easy bruising.

Published in:

2019

By:

Power, Bradley;
Ferreira, Carlos R.;
Chen, Dong;
Zein, Wadih M.;
O'Brien, Kevin J.;
Introne, Wendy J.;
Stephen, Joshi;
Gahl, William A.;
Huizing, Marjan;
Malicdan, May Christine V.;
Adams, David R.;
Gochuico, Bernadette R.

Publication type:

journal article

Hermansky-Pudlak syndrome type 2 manifests with fibrosing lung disease early in childhood.

Published in:

2018

By:

Hengst, Meike;
Naehrlich, Lutz;
Mahavadi, Poornima;
Grosse-Onnebrink, Joerg;
Terheggen-Lagro, Suzanne;
Skanke, Lars Høsøien;
Schuch, Luise A.;
Brasch, Frank;
Guenther, Andreas;
Reu, Simone;
Ley-Zaporozhan, Julia;
Griese, Matthias;
Skanke, Lars Høsøien

Publication type:

journal article

Coexistence of Hermansky-Pudlak syndrome and JAK2<sup>V617F</sup>-positive essential thrombocythemia.

Published in:

Ultrastructural Pathology, 2019, v. 43, n. 1, p. 94, doi. 10.1080/01913123.2019.1593269

By:

Eskazan, Tugce;
Erturkuner, Salime Pelin;
Isildar, Basak;
Eskazan, Ahmet Emre;
Ar, Muhlis Cem;
Atay, Kadri;
Baslar, Zafer;
Tasyurekli, Mustafa

Publication type:

Article

Hermansky-Pudlak Sendromlu Bir Olguya ait Klinik Özellikler.

Published in:

Gulhane Medical Journal, 2013, v. 55, n. 2, p. 146, doi. 10.5455/gulhane.39840

By:

Türk, Adem;
Fidan, Sami;
Uzun, Yusuf;
Ersöz, şafak

Publication type:

Article

Case Report : Hermansky Pudlak Syndrome (Presenting as late onset heavy Menstrual Bleeding).

Published in:

2013

By:

RAY, AMITA;
RAY, SUJOY;
MATTHEW, JOSE JOHN

Publication type:

Case Study

Hermansky-Pudlak Syndrome: A Case Report.

Published in:

2014

By:

Berber, Ilhami;
Erkurt, Mehmet Ali;
Kuku, Irfan;
Kaya, Emin;
Koroglu, Mustafa;
Nizam, Ilknur;
Gul, Mehmet;
Bentli, Recep

Publication type:

Case Study

Hermansky–Pudlak syndrome pulmonary fibrosis: a rare inherited interstitial lung disease.

Published in:

European Respiratory Review, 2021, v. 30, n. 159, p. 1, doi. 10.1183/16000617.0193-2020

By:

Tadafumi Yokoyama;
Gochuico, Bernadette R.

Publication type:

Article

Association of the Hermansky--Pudlak syndrome type 4 (HPS4) gene variants with cognitive function in patients with schizophrenia and healthy subjects.

Published in:

BMC Psychiatry, 2013, v. 13, n. 1, p. 549, doi. 10.1186/1471-244X-13-276

By:

Go Kuratomi;
Atsushi Saito;
Yuji Ozeki;
Takashi Watanabe;
Kumiko Fujii;
Kazutaka Shimoda;
Toshihiko Inukai;
Harunobu Mori;
Kenichi Ohmori;
Kazufumi Akiyama

Publication type:

Article

Cellular and molecular defects in a patient with Hermansky-Pudlak syndrome type 5.

Published in:

PLoS ONE, 2017, v. 12, n. 3, p. 1, doi. 10.1371/journal.pone.0173682

By:

Stephen, Joshi;
Yokoyama, Tadafumi;
Tolman, Nathanial J.;
O’Brien, Kevin J.;
Nicoli, Elena-Raluca;
Brooks, Brian P.;
Huryn, Laryssa;
Titus, Steven A.;
Adams, David R.;
Chen, Dong;
Gahl, William A.;
Gochuico, Bernadette R.;
Malicdan, May Christine V.

Publication type:

Article

Immunophenotypic and Ultrastructural Analysis of Mast Cells in Hermansky-Pudlak Syndrome Type-1: A Possible Connection to Pulmonary Fibrosis.

Published in:

PLoS ONE, 2016, v. 11, n. 7, p. 1, doi. 10.1371/journal.pone.0159177

By:

Kirshenbaum, Arnold S.;
Cruse, Glenn;
Desai, Avanti;
Bandara, Geethani;
Leerkes, Maarten;
Lee, Chyi-Chia R.;
Fischer, Elizabeth R.;
O’Brien, Kevin J.;
Gochuico, Bernadette R.;
Stone, Kelly;
Gahl, William A.;
Metcalfe, Dean D.

Publication type:

Article

Hermansky-Pudlak syndrome subtype 5 (HPS-5) novel mutation in a 65 year-old with oculocutaneous hypopigmentation and mild bleeding diathesis: The importance of recognizing a subtle phenotype.

Published in:

Platelets, 2018, v. 29, n. 1, p. 91, doi. 10.1080/09537104.2017.1361019

By:

Botero, Juliana Perez;
Chen, Dong;
Majerus, Julie A.;
Coon, Lea M.;
He, Rong;
Warad, Deepti M.;
Pruthi, Rajiv K.;
Nichols, William L.

Publication type:

Article

Metastatic Cutaneous Involvement of Granulomatous Colitis in Hermansky-Pudlak Syndrome.

Published in:

Pediatric Dermatology, 2013, v. 30, n. 6, p. e278, doi. 10.1111/j.1525-1470.2012.01728.x

By:

Weitz, Nicole;
Patel, Vishal;
Tlougan, Brook;
Mencin, Ali;
Kadenhe‐Chiweshe, Angela;
Morel, Kimberly D.;
Lauren, Christine

Publication type:

Article

Characterization of melanosomes and melanin in Japanese patients with Hermansky–Pudlak syndrome types 1, 4, 6, and 9.

Published in:

Pigment Cell & Melanoma Research, 2018, v. 31, n. 2, p. 267, doi. 10.1111/pcmr.12662

By:

Okamura, Ken;
Abe, Yuko;
Araki, Yuta;
Wakamatsu, Kazumasa;
Seishima, Mariko;
Umetsu, Takafumi;
Kato, Atsushi;
Kawaguchi, Masakazu;
Hayashi, Masahiro;
Hozumi, Yutaka;
Suzuki, Tamio

Publication type:

Article

Identification and clinical characterization of Hermansky-Pudlak syndrome alleles in the Pakistani population.

Published in:

Pigment Cell & Melanoma Research, 2016, v. 29, n. 2, p. 231, doi. 10.1111/pcmr.12438

By:

Yousaf, Sairah;
Shahzad, Mohsin;
Kausar, Tasleem;
Sheikh, Shakeel A.;
Tariq, Nabeela;
Shabbir, Asra S.;
Ali, Muhammad;
Waryah, Ali M.;
Shaikh, Rehan S.;
Riazuddin, Saima;
Ahmed, Zubair M.

Publication type:

Article

Clinical management and outcomes of patients with Hermansky-Pudlak syndrome pulmonary fibrosis evaluated for lung transplantation.

Published in:

PLoS ONE, 2018, v. 13, n. 3, p. 1, doi. 10.1371/journal.pone.0194193

By:

El-Chemaly, Souheil;
O’Brien, Kevin J.;
Nathan, Steven D.;
Weinhouse, Gerald L.;
Goldberg, Hilary J.;
Connors, Jean M.;
Cui, Ye;
Astor, Todd L.;
Jr.Camp, Philip C.;
Rosas, Ivan O.;
Lemma, Merte;
Speransky, Vladislav;
Merideth, Melissa A.;
Gahl, William A.;
Gochuico, Bernadette R.

Publication type:

Article

Unexpected intra-operative bleeding due to Hermansky- Pudlak Syndrome.

Published in:

2015

By:

Ozgur, Mustafa;
Yilmaz, Bahar

Publication type:

Case Study

A deletion in the Hermansky-Pudlak syndrome 4 ( Hps4) gene appears to be responsible for albinism in channel catfish.

Published in:

Molecular Genetics & Genomics, 2017, v. 292, n. 3, p. 663, doi. 10.1007/s00438-017-1302-8

By:

Li, Yueru;
Geng, Xin;
Bao, Lisui;
Elaswad, Ahmed;
Dunham, Rex;
Liu, Zhanjiang;
Huggins, Kevin

Publication type:

Article

A novel likely pathogenic variant in a patient with Hermansky-Pudlak syndrome.

Published in:

Cold Spring Harbor Molecular Case Studies, 2021, v. 7, n. 5, p. 1, doi. 10.1101/mcs.a006110

By:

Lansdon, Lisa A.;
Dong Chen;
Rush, Eric T.;
Engleman, Kendra;
Lei Zhang;
Saunders, Carol J.;
Oroszi, Gabor

Publication type:

Article

Hermansky-Pudlak syndrome genes are frequently mutated in patients with albinism from the Arabian Peninsula.

Published in:

Clinical Genetics, 2016, v. 90, n. 1, p. 96, doi. 10.1111/cge.12715

By:

Khan, A. O.;
Tamimi, M.;
Lenzner, S.;
Bolz, H. J.

Publication type:

Article

Chitinase 3-like-1 and its receptors in Hermansky-Pudlak syndrome--associated lung disease.

Published in:

Journal of Clinical Investigation, 2015, v. 125, n. 8, p. 3178, doi. 10.1172/JCI79792

By:

Yang Zhou;
Chuan Hua He;
Herzog, Erica L.;
Xueyan Peng;
Chang-Min Lee;
Nguyen, Tung H.;
Gulati, Mridu;
Gochuico, Bernadette R.;
Gahl, William A.;
Slade, Martin L.;
Chun Geun Lee;
Elias, Jack A.

Publication type:

Article

Poster 494 An Unusual Cause of Ischemic Stroke in a Patient With Hermansky‐Pudlak Syndrome: A Case Report.

Published in:

2011

By:

Desai, Anjuli;
Nissley, Frederick;
Peoples, James;
Siu, Gilbert

Publication type:

Abstract

The pink gene encodes the Drosophila orthologue of the human Hermansky–Pudlak syndrome 5 (HPS5) gene.

Published in:

Genome, 2007, v. 50, n. 6, p. 548, doi. 10.1139/G07-032

By:

Syrzycka, Monika;
McEachern, Lori A.;
Kinneard, Jennifer;
Prabhu, Kristel;
Fitzpatrick, Kathleen;
Schulze, Sandra;
Rawls, John M.;
Lloyd, Vett K.;
Sinclair, Donald A. R.;
Honda, Barry M.

Publication type:

Article

Novel mutation in Hermansky-Pudlak syndrome type 2 with mild immunological phenotype.

Published in:

Platelets, 2013, v. 24, n. 7, p. 538, doi. 10.3109/09537104.2012.741275

By:

Kurnik, Karin;
Bartsch, Ingrid;
Maul-Pavicic, Andrea;
Ehl, Stephan;
Sandrock-Lang, Kirstin;
Bidlingmaier, Christoph;
Rombach, Nina;
Busse, Anja;
Belohradsky, Bernd H.;
Müller-Höcker, Josef;
Aslanidis, Charalampos;
Schmitz, Gerd;
Zieger, Barbara

Publication type:

Article

A novel mutation in a Turkish patient with Hermansky–Pudlak syndrome type 5.

Published in:

European Journal of Haematology, 2008, v. 80, n. 4, p. 356, doi. 10.1111/j.1600-0609.2007.01024.x

By:

Korswagen, Lindy-Anne;
Huizing, Marjan;
Simsek, Suat;
Janssen, Jeroen J. W. M.;
Zweegman, Sonja

Publication type:

Article

Simple chronic colitis model using hypopigmented mice with a Hermansky-Pudlak syndrome 5 gene mutation.

Published in:

Pigment Cell & Melanoma Research, 2016, v. 29, n. 5, p. 578, doi. 10.1111/pcmr.12504

By:

Itoh, Yumi;
Nagaoka, Yasuo;
Katakura, Yoshio;
Kawahara, Hidehisa;
Takemori, Hiroshi

Publication type:

Article

Case report: Inflammatory bowel disease in Hermansky-Pudlak syndrome type 3 due to novel variant in HPS3.

Published in:

Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1465527

By:

Mai, Jingqun;
Zhang, Zhu;
Xu, Bocheng;
Liu, Shanling;
Wang, He;
Wang, Hao;
Yang, Shuo

Publication type:

Article

Iga nephropathy, antineutrophil cytoplasmic antibodies and crescentic glomerulonephritis in a patient with the Hermansky-Pudlak syndrome.

Published in:

2001

By:

Tagboto, Senyo;
Carr, Sue;
Varghese, Anitha;
Allen, Alice;
Feehally, John;
Furness, Peter;
Tagboto, S;
Carr, S;
Varghese, A;
Allen, A;
Feehally, J;
Furness, P

Publication type:

journal article

Crohn's-like colitis, enterocolitis and perianal disease in Hermansky–Pudlak syndrome.

Published in:

Colorectal Disease, 2006, v. 8, n. 7, p. 539, doi. 10.1111/j.1463-1318.2006.01046.x

By:

Hazzan, D.;
Seward, S.;
Stock, H.;
Zisman, S.;
Gabriel, K.;
Harpaz, N.;
Bauer, J. J.

Publication type:

Article

Sequence-Based Mapping and Genome Editing Reveal Mutations in Stickleback Hps5 Cause Oculocutaneous Albinism and the casper Phenotype.

Published in:

G3: Genes | Genomes | Genetics, 2017, v. 7, n. 9, p. 3123, doi. 10.1534/g3.117.1125

By:

Hart, James C.;
Miller, Craig T.

Publication type:

Article

Dermatologic manifestations in patients with the Hermansky-Pudlak syndrome types 1 and 3.

Published in:

2022

By:

Santos Malave, Gabriel;
Izquierdo, Natalio J.;
Sanchez, Nestor P.

Publication type:

journal article

High Frequency of Hermansky–Pudlak Syndrome Type 1 (HPS1) Among Japanese Albinism Patients and Functional Analysis of HPS1 Mutant Protein.

Published in:

Journal of Investigative Dermatology, 2005, v. 125, n. 4, p. 715, doi. 10.1111/j.0022-202X.2005.23884.x

By:

Ito, Shiro;
Suzuki, Tamio;
Inagaki, Katsuhiko;
Suzuki, Noriyuki;
Takamori, Kenji;
Yamada, Tomoko;
Nakazawa, Mitsuru;
Hatano, Michihiro;
Takiwaki, Hirotsugu;
Kakuta, Yumi;
Spritz, Richard A.;
Tomita, Yasushi

Publication type:

Article

Report of Hermansky–Pudlak Syndrome in Two Families with Novel Variants in HPS3 and HPS4 Genes.

Published in:

Genes, 2023, v. 14, n. 1, p. 145, doi. 10.3390/genes14010145

By:

Zaman, Qaiser;
Sadeeda;
Anas, Muhammad;
Rehman, Gauhar;
Khan, Qadeem;
Iftikhar, Aiman;
Ahmad, Mashal;
Owais, Muhammad;
Ahmad, Ilyas;
Muthaffar, Osama Yousef;
Abdulkareem, Angham Abdulrhman;
Bibi, Fehmida;
Jelani, Musharraf;
Naseer, Muhammad Imran

Publication type:

Article

Hermansky-Pudlak Syndrome Complicated by Crohn's Disease and Hidradenitis Suppurativa: A Case of Multisystem Immune Dysregulation.

Published in:

ACG Case Reports Journal, 2025, v. 12, n. 4, p. 1, doi. 10.14309/crj.0000000000001647

By:

Yanofsky, Russell;
Stein, Sarah L.;
Rubin, David T.;
Kellar, Amelia

Publication type:

Article

Pulmonary Fibrosis in Hermansky-Pudlak Syndrome.

Published in:

2016

By:

Vicary, Glenn W.;
Vergne, Yeidyly;
Santiago-Cornier, Alberto;
Young, Lisa R.;
Roman, Jesse

Publication type:

journal article

After an initial Hermansky–Pudlak syndrome clinical diagnosis, molecular testing reveals variants for oculocutaneous albinism type 1B: A case report.

Published in:

2024

By:

Serrano‐González, Joseline;
Montes‐Rodríguez, Ingrid;
Renta, Jessicca Y.;
Rojas, Ricardo;
Cadilla, Carmen L.

Publication type:

Case Study

Dysregulated myosin in Hermansky-Pudlak syndrome lung fibroblasts is associated with increased cell motility.

Published in:

2022

By:

Imani, Jewel;
Bodine, Steven P. M.;
Lamattina, Anthony M.;
Ma, Diane D.;
Shrestha, Shikshya;
Maynard, Dawn M.;
Bishop, Kevin;
Nwokeji, Arinze;
Malicdan, May Christine V.;
Testa, Lauren C.;
Sood, Raman;
Stump, Benjamin;
Rosas, Ivan O.;
Perrella, Mark A.;
Handin, Robert;
Young, Lisa R.;
Gochuico, Bernadette R.;
El-Chemaly, Souheil

Publication type:

journal article

HERMANSKY-PUDLAK SYNDROME; A CASE REPORT WITH ANALYSIS OF AUTO-FLUORESCENT CEROID-LIKE PIGMENTS.

Published in:

Gerontology, 1995, v. 41, n. S2, p. 297, doi. 10.1159/000213751

By:

Ohbayashi, C.;
Kanomata, N.;
Imai, Y.;
Ito, H.;
Shimasaki, H.

Publication type:

Article

Pulmonary Fibrosis in Hermansky-Pudlak Syndrome.

Published in:

Respiration, 2006, v. 73, n. 3, p. 382, doi. 10.1159/000091609

By:

Pierson, Diane M.;
Ionescu, Diana;
Gefei Qing;
Yonan, Abdullah M.;
Parkinson, Kent;
Colby, Thomas C.;
Leslie, Kevin

Publication type:

Article

Granulomatous Colitis Due to Hermansky-Pudlak Syndrome.

Published in:

ACG Case Reports Journal, 2024, v. 11, n. 11, p. 1, doi. 10.14309/crj.0000000000001477

By:

Koulali, Hajar;
Azzmouri, Samira;
Tajir, Mariam;
Zerrouki, Khawla;
Haloui, Anass;
Elmqaddem, Ouiam;
Zazour, Abdelkrim;
Ismaili, Zahi;
Kharrasse, Ghizlane

Publication type:

Article

A new case with Hermansky-Pudlak syndrome type 9, a rare cause of syndromic albinism with severe defect of platelets dense bodies.

Published in:

Platelets, 2021, v. 32, n. 3, p. 420, doi. 10.1080/09537104.2020.1742315

By:

Michaud, Vincent;
Fiore, Mathieu;
Coste, Valentine;
Huguenin, Yoann;
Bordet, Jean-Claude;
Plaisant, Claudio;
Lasseaux, Eulalie;
Morice-Picard, Fanny;
Arveiler, Benoit

Publication type:

Article